Gmp Qtopic380 pirkti naudotą (126)

Gamybos metai: 2018, būklė: naudotas, Cette annonce concerne un fermenteur Solaris Biotech Solution Jupiter 3.0. L’unité est en parfait état de fonctionnement et immédiatement disponible. Le Solaris Biotech Solution Jupiter 3.0 Fermentor est un bioréacteur hautement polyvalent et configurable, parfaitement adapté aux applications à l’échelle du laboratoire. Grâce à son automatisation avancée et à sa conception robuste, il répond aussi bien aux besoins de recherche et développement qu’à ceux de la petite production. Caractéristiques principales : Conception autoclavable et stérilisable : Permet un nettoyage facile, une stérilité optimale et une exploitation fiable pour des processus sans contamination. Cuves flexibles : Disponibles avec différents rapports hauteur/diamètre et systèmes de thermorégulation, volumes totaux de 2,0 L à 10,0 L. Contrôle de la pression : Gère des pressions jusqu’à 1,6 bar dans les cuves à double enveloppe de 2 L et 4 L, avec flux continu de gaz entrant et sortant. Logiciel SCADA innovant (LEONARDO 3.0) : Gestion automatisée des processus de fermentation et de culture, garantissant précision et facilité d’utilisation. Gestion parallèle : Permet l’exploitation simultanée de jusqu’à 24 unités à partir d’une seule interface HMI dotée d’un écran 24”, simplifiant la gestion de tâches complexes. Accès à distance : Surveillance et contrôle via PC, tablette ou smartphone par scan de QR code ou portail web dédié, pour une gestion à distance facilitée. Applications : Développement et optimisation de procédés : Facilite l’expérimentation et l’optimisation des bioprocédés pour études d’échelle. Enseignement et recherche : Convient à la formation et à la recherche fondamentale en bioprocédés. Lodpoxxz T Hjfx Apnjhn Production à petite échelle : Prend en charge la fabrication en petits lots et les productions pilotes. Avantages : Performance économique : Des fonctionnalités avancées à un coût maîtrisé pour laboratoires et environnements de production. Automatisation poussée : Gestion simplifiée de la fermentation et de la culture grâce au logiciel LEONARDO 3.0, avec une réduction de la charge opérateur. Polyvalence et configurabilité : S’adapte à de nombreuses applications tout en assurant la conformité aux normes GMP validées. Spécifications techniques : - Matériaux : Résine VALOX (externe) et silicone (interne) - Autoclavable : 121-133°C, jusqu’à 30 minutes - Volume résiduel : 0,04 mL - Débit : 65 mL/min

Būklė: naujas, Gamybos metai: 2020, Funkcionalumas: visiškai funkcionalus, Įranga: dokumentacija / vadovas, Brinox LEP 11 – Pharmaceutical Chromatography System with CIP System New, unused, original packaging Manufacturer: Brinox Model: LEP 11 Configuration: PP6711 with associated CIP unit CS6711 Condition: New – unused – factory sealed (Factory New Condition) Description For sale is a Brinox LEP 11 pharmaceutical chromatography system, comprising the chromatography panel PP6711 and the associated CIP unit CS6711. Lhedpfx Asyl Ndnspnsn The system is completely new, unused, and in its original packaging. It was engineered, manufactured, and delivered, but never installed or commissioned. The unit is designed for C1-INH chromatography and is intended for controlled protein purification using sieve bottom vessels in a GMP environment. Process Functions - Transfer of loaded QAE gel (slurry) - Washing and elution processes - Transfer of eluate to pre-precipitation vessels - Gel disposal via container station - Fully automatic CIP and SIP cleaning Technical Data - Fully CIP and SIP capable - Design pressure: –0.9 to +6 bar - Design temperature: +2 °C to +95 °C - Flow rates up to 10 m³/h - Adjustable slurry delivery 0.2 – 3 m³/h Specification - Product-contact parts stainless steel 1.4435 - Electropolished Ra ≤ 0.8 µm - FDA and EU compliant seals - Residual drainable construction - Cleanroom panel with Tri-Clamp connections - Magnetically monitored connection bend sections - 0.2 µm vent filter CIP Unit CS6711 - Compact stainless steel skid - Centrifugal pump - Shell-and-tube heat exchanger - Adjustable operating pressure - GMP compliant design The system is in factory new condition and has never been in production use.

Būklė: labai geros būklės (naudotas), Funkcionalumas: visiškai funkcionalus, Gamybos metai: 2016, Model Slugger mit 12 Stationen und Spezialwerkzeugen. Maximale Presskraft von 120 kN. 16/20 Stationen verfügbar mit D-Werkzeugen und 100 kN Presskraft. Quadratisches Modell in GMP-Ausführung. Optional elektromagnetische Kupplung für Non-Pharma-/Heavy-Duty-Anwendungen; AC-Frequenzumrichter (ACVFD) als Option für den Hauptantrieb. Hochleistungsmotor für Slugging-Anwendungen. Lhsdorrgtrspfx Apnon Ideal für Slugging-/Brausetabletten-/Veterinär-/Nicht-Pharma-Anwendungen. Kraftmessdose zur Überwachung der Presskraft optional erhältlich. 38 mm Rundtabletten können problemlos gepresst werden.

Būklė: naujas, Gamybos metai: 2020, Funkcionalumas: visiškai funkcionalus, Įranga: dokumentacija / vadovas, Package 15 PP6715 – CS6715 Brinox LEP 11 – Pharma Chromatography and CIP System New – Factory Sealed – Factory New Manufacturer: Brinox Model: LEP 11 Configuration: PP6715 with CIP System CS6715 Condition: New, unused, original packaging Description Lsdpfeyl Rqpex Apnehn For sale is a high-quality pharmaceutical chromatography system Brinox LEP 11 consisting of panel PP6715 and the associated CIP unit CS6715. The system is completely new, unused, and in the original manufacturer condition. It was designed for industrial C1-INH chromatography and complies with the highest GMP standards. Functionality - Slurry transfer - Washing and elution processes - Transfer to pre-precipitation tanks - Gel disposal - Autonomous CIP circuit Technical Specifications - Wetted parts: stainless steel 1.4435 - Electropolished, Ra ≤ 0.8 µm - FDA-compliant sealing systems - Suitable for CIP/SIP - Operating pressure up to 6 bar - Temperature range up to 95 °C - Completely drainable piping CIP Skid CS6715 - Stainless steel frame - Centrifugal pump - Shell-and-tube heat exchanger - Cleaning media temperature control - Adjustable supply pressure The system is in mint factory condition with zero operating hours.

Būklė: naujas, Gamybos metai: 2020, Funkcionalumas: visiškai funkcionalus, bakelio talpa: 3 500 l, Įranga: dokumentacija / vadovas, BRINOX 3,500 L Storage Tank – 1.4435 – Double Jacket – PED Module G – TÜV SÜD – FAT – 2020 – As New Manufacturer: BRINOX d.o.o. Type: SVBBHI-3500 Tag No.: BH6772-BH1001 Package 30 Serial Number: 1003462 Year of Manufacture: 2020 Condition: As new / unused TECHNICAL DATA Product Type: Storage tank / process vessel Nominal volume: 3,500 liters Total volume: 4,082 liters Jacket volume: 226 liters Empty weight: approx. 1,760 kg Product contact material: 1.4435 (AISI 316L pharmaceutical grade) Jacket material: 1.4404 CE Marking: CE 0036 Permissible pressure PS vessel: -1 / +3 bar Permissible pressure PS jacket: -1 / +6 bar Test pressure PT vessel: 5.6 bar Test pressure PT jacket: 10.8 bar Permissible temperature TS: -10 °C to +150 °C Fluid group: 2 Design according to AD 2000 code Pressure vessel in accordance with PED 2014/68/EU Category IV Module G – Individual inspection Notified body: TÜV SÜD Industrie Service GmbH (identification number 0036) TÜV approval including design review, final inspection, and pressure test fully documented. FAT – Factory Acceptance Test The vessel has been fully tested and released ex works. Tests carried out include: • Pressure test according to PED • Design review by TÜV SÜD • Visual inspection of all weld seams • Non-destructive tests (RT, PT) • Dimensional and drawing verification (as-built) • Verification of material certificates • Calibration test of pressure gauges • Verification of marking • Documentation check according to inspection list Complete FAT and TÜV protocols available. EXECUTION • Cylindrical, horizontal storage vessel • Double jacket for heating/cooling • High-quality pharmaceutical design • Manway with round pressure closure • CIP pipe system • J-pipe / internal piping • Sight glass DN80 • Multiple spare and process connections • Biocontrol flanges • Heavy-duty bearing blocks / trunnion design • Lifting lugs • Nameplate with full PED identification DOCUMENTATION – completely and systematically available • EU Declaration of Conformity • TÜV certificate with acceptance report (Module G) • TÜV design inspection and certification • Material certificates 3.1 • Welders’ lists and work samples • Non-destructive test reports (RT, PT) • Dimensional inspection reports • Calibration reports for pressure gauges • Surface and manufacturing reports • Parts list • Detail drawings (body, lid, CIP, J-pipe, etc.) • Operating and maintenance documents Complete digital documentation file available. CONDITION Lhodpfxsylnwyj Apnen • Never used in production • Warehouse item • Interior as new • No corrosion • No signs of use • Industrial new condition • Immediately available SUITABLE FOR • Pharmaceutical solutions • WFI / PW systems • Buffer and media preparation • Chemical media • GMP production plants • Process and waste treatment plants SPECIAL FEATURE High-quality BRINOX pharmaceutical manufacturing with full PED Module G individual inspection by TÜV SÜD, CE 0036 marking, and documented FAT testing. Not a standard tank – this is certified project quality with comprehensive GMP-compliant documentation.

Būklė: naudotas, didžiausias leistinas svoris: 32 540 kg, bendras svoris: 39 000 kg, ašių konfigūracija: 3 ašys, pirmoji registracija: 06/2023, kita apžiūra (TÜV): 06/2026, krovinio erdvės tūris: 50 m³, bendras plotis: 2 550 mm, bendras aukštis: 3 710 mm, Gamybos metai: 2023, Įranga: ABS,

Būklė: naujas, Gamybos metai: 2020, Funkcionalumas: visiškai funkcionalus, bakelio talpa: 3 200 l, Įranga: dokumentacija / vadovas, BRINOX 3,200 L Solution Tank – 316L – Double Jacket – TÜV / PED Module G – FAT – 2020 – As New Manufacturer: BRINOX d.o.o. Tag-No.: BH6761-BH1001 Serial Number: 1003446 Year of Manufacture: 2020 Condition: As new / unused Technical Data Product type: ELUTION / Solution Tank Volume: 3,200 litres Empty weight: 1,815 kg Material: 1.4404 (AISI 316L) CE marking: CE 0036 Tank Pressure Operating pressure: -1 / +3 bar Test pressure: 4.6 bar Jacket Pressure (heating/cooling jacket) Operating pressure: -1 / +6 bar Test pressure: 10.8 bar Temperature range: -20 °C to +150 °C Pressure vessel according to PED 2014/68/EU Module G – Individual assessment Notified body: TÜV SÜD (registration number 0036) Permitted number of load cycles: 7300 / 5475 at pressure fluctuation range 3.3 / 4.5 bar TÜV / PED / FAT • EU certificate of conformity according to 2014/68/EU • Certificate Number: Z-EU-SI-LJU-20-08-2350154-14124056 • Test report available • Pressure test with water successfully completed • Final inspection by TÜV SÜD Industrie Service GmbH • Factory Acceptance Test (FAT) performed • Module G individual approval • Complete Turn-Over-Package (TOP) included Full documentation available The complete technical documentation package is available, including: • EU Declaration of Conformity and Warranty Certificates • TÜV certificate with inspection report • TÜV design review and certification • Nameplate documentation • Assembly drawings • Part drawings • Welder lists and welding procedure qualifications • Work samples • Analysis certificates of welding consumables • Analysis certificates of welding gases • Manufacturer qualification certificate • Non-destructive testing (NDT) reports • Material certificates (3.1) • Calibration certificates • Internal pressure test report • Dimensional accuracy inspection • Surface roughness protocol Lhsdpfsykkbxsx Apnen • Surface treatment report • Operating and maintenance manuals (equipment and components) Scope of documentation meets project standard for pharmaceutical systems. Design • Double jacket for heating and cooling • Fully made of stainless steel 316L (1.4404) • High-gloss polished internal surface • Pharmaceutical-grade weld seams • CIP/SIP-capable connections • Multiple manholes / inspection ports • Clamp and flange connections • Instrumentation prepared (pressure, temperature, sensors) • Heavy-duty project construction • Lifting lugs for crane handling • PED-compliant pressure design Condition • Never used in production • Stock item from project surplus • Interior absolutely clean • No corrosion • No signs of use • Industrial as-new condition • Immediately available Suitable for • Pharmaceutical solutions • WFI / PW systems • Elution / buffer preparation • Sterile liquid processes • Biotechnology • GMP production facilities • CIP media Special feature This is not a standard tank, but a premium BRINOX project fabrication in genuine pharmaceutical quality, featuring: • PED Module G individual assessment • TÜV SÜD acceptance • FAT performed • Complete welding, material, and inspection documentation • Documented surface treatment • 316L execution for sterile applications Project-grade quality for demanding GMP applications – immediately available.

Gamybos metai: 2017, būklė: beveik kaip naujas (parodų įrenginys), Funkcionalumas: visiškai funkcionalus, Pharmatec Syntegon SVP 250 LF – Formulation System for Sterile and Aseptic Liquid Pharmaceuticals For sale: Pharmatec Syntegon SVP 250 LF formulation system for Small Volume Parenterals (SVP). Sale is carried out on behalf of Syntegon (manufacturer, formerly Bosch Packaging/Pharmatec GmbH, Dresden). Technical Specifications: - Suitable for aqueous solutions, suspensions, and emulsions - Flexible process adaptation: terminal sterilization, sterile filtration, aseptic compounding - 2-vessel system for batch sizes from 25–250 L (expandable to up to 4 vessels) - Auxiliary substances can be dosed via manway under LAF or by pumping system - High-potency active ingredients (OEB4/OEB5) possible via high-containment valve - CIP/SIP interfaces and prefabricated automation for integration with filling lines - GMP-compliant design, suitable for cleanroom classes Pricing: - Special price: please submit your offer - Original price in 2018: approx. €1,050,000 - Current list price of comparable systems in 2025/2026: €1,415,000 Completion Status & Lead Time: - The system is currently not fully operational, as the automation system including software needs to be reinstalled and certain components replaced. Lodpfxjxdy Ere Apnjhn - Completion takes place directly at the manufacturer Syntegon after agreement – lead time approx. 3–4 months. - For comparison: delivery time for a new system is approx. 12 months. Special Features: - System was originally built for trade fair purposes (demonstration unit) - Sale is conducted directly on behalf of Syntegon, the original manufacturer - Ideal for pharmaceutical companies looking for a flexible and high-performance SVP system with moderate lead time.

Gamybos metai: 2020, būklė: naujas, Funkcionalumas: visiškai funkcionalus, Įranga: dokumentacija / vadovas, Package 14 PP6713 – CS6713 Brinox LEP 11 – GMP Chromatography System with CIP Skid New – unused – original packaging Manufacturer: Brinox Model: LEP 11 Version: PP6713 with CIP System CS6713 Lhedpfxjyl Rnnj Apnsn Condition: New – in original packaging – never installed Description Offered is a pharmaceutical chromatography system LEP 11, consisting of the chromatography panel PP6713 and the corresponding CIP skid CS6713. The system is completely new, unused, and in its original manufacturer condition. The unit was designed for GMP protein purification within C1-INH chromatography processes. Plant Technology - Cleanroom panel for wall integration - Transfer lines to false-bottom vessels - Precipitation vessel connection - Gel waste line - Complete utility piping Technical Specifications - Design pressure: –0.9 to +6 bar - Design temperature: +2 to +95 °C - Electropolished surfaces Ra ≤ 0.8 µm - Material: 1.4435 (stainless steel) - Fully drainable - GMP compliant design CIP System CS6713 - Stainless steel frame construction - Centrifugal pump - Shell-and-tube heat exchanger - Conductivity, pressure, and temperature monitoring - Adjustable CIP feed The system is factory-new and has never been commissioned.

Būklė: naujas, Gamybos metai: 2020, Funkcionalumas: visiškai funkcionalus, bakelio talpa: 3 200 l, Įranga: dokumentacija / vadovas, BRINOX 3,200 L Solution Tank – 316L Stainless Steel – Double Jacket – TÜV / PED Module G – FAT – 2020 – Like New Package 17 Manufacturer: BRINOX d.o.o. Tag No.: BH6762-BH1001 Year of Manufacture: 2020 Condition: Like new / unused TECHNICAL DATA Type: ELUTION / Solution Tank Capacity: 3,200 liters Material: 1.4404 (AISI 316L) CE marking: Present (CE 0036) Tank Pressure: Operating pressure: -1 / +3 bar Test pressure: According to TÜV inspection Jacket Pressure (Heating/Cooling Jacket): Operating pressure: -1 / +6 bar Test pressure: According to TÜV inspection Temperature range: -20 °C to +150 °C Pressure vessel in accordance with PED 2014/68/EU Module G – Individual inspection Acceptance by notified body (number 0036) FAT – Factory Acceptance Test The tank was tested as part of a documented FAT. The inspections included, among others: • Welding documentation review • Visual inspection of weld seams • Leak testing • Pressure testing • Surface roughness measurement • Calibration test of sensors • Layout and dimensional check • Documentation review Comprehensive FAT report including test records available in full. DESIGN FEATURES • Double jacket for heating/cooling • Completely made from 316L stainless steel • Mirror-polished interior surface • Pharmaceutical-grade weld seams • CIP/SIP-capable connections • Multiple manways / inspection ports • Clamp and flange connections • Instrumentation prepared (pressure, temperature, sensors) • Heavy-duty project execution • Lifting lugs for crane handling CONDITION • Never used in production • Warehouse surplus from project stock • Interior absolutely clean • No corrosion • No signs of use • Industrial as-new condition • Immediately available Lhodjykkhropfx Apnsn DOCUMENTATION – complete and structured A comprehensive, project-specific quality and manufacturing documentation is available for the tank, including: • EU Declaration of Conformity and warranty certificates • TÜV certificate with acceptance report • TÜV design review and certification • Material certificates (3.1) • Welder lists and welding procedure qualifications (WPQR/WPS) • Non-destructive testing (NDT) reports • Analysis certificates for welding consumables and shielding gas • Surface roughness report • Surface treatment report • Dimensional accuracy inspection • Internal pressure test • Calibration certificates • Assembly documentation • Part drawings • Operating and maintenance manuals Complete documentation folder available digitally. SUITABLE FOR • Pharmaceutical solutions • WFI / PW systems • Elution / buffer preparation • Sterile liquid processes • Biotechnology • GMP production facilities • CIP media SPECIAL FEATURE This is not a standard tank but a high-specification, BRINOX project-built vessel in true pharmaceutical quality, featuring validated pressure design, full PED compliance (Module G), documented FAT inspection, and comprehensive quality documentation. Project-grade equipment for sterile applications – immediately available.

Gamybos metai: 2018, būklė: naudotas, Šis įrašas skirtas GE Healthcare UniFlux 120 srauto krypties filtracijos (TFF) sistemai. Įrenginys pilnai veikiantis ir paruoštas nedelsiam perdavimui. GE Healthcare UniFlux 120 – tai pilnai automatizuota srauto krypties filtracijos (TFF) sistema, skirta skaidrinimo, koncentravimo bei diafiltravimo užduotims bandomosiose ir pramoninėse gamybos fazėse. UniFlux 120, kurio srauto diapazonas siekia nuo 12 iki 120 litrų per minutę, idealiai tinka biotechnologiniams procesams, tokiems kaip monokloninių antikūnų gryninimas, vakcinų gamyba ir baltymų koncentravimas. Pagrindiniai privalumai ir ypatybės: - Pilnai automatinis veikimas – Sistema valdoma UNICORN programine įranga, užtikrinančia vientisą duomenų registravimą, proceso automatizavimą ir atitikimą reglamentams. - Universalios filtracijos galimybės – Galima naudoti kasečių arba pluoštinių membranų formatą. Perėjimas tarp formatų galimas, pirminei kasečių laikiklio instaliacijai būtinas Cytiva servisas. - Aukšto našumo filtracija – Rotacinis mentinis siurblys užtikrina tikslų srauto valdymą ir optimizuoja filtracijos našumą. - Higieniškas ir GMP reikalavimus atitinkantis dizainas – Iš nerūdijančio plieno, todėl puikiai tinka farmacijos ir biotechnologijų pramonei. - Skalabilumas ir patikimumas – Sistema sukurta procesų kūrimui ir plėtrai iki pramoninės gamybos, užtikrinant pastovų filtracijos procesą. Pritaikymo sritys: - Biofarmacijos procesai - Monokloninių antikūnų gryninimas - Vakcinų gamyba - Baltymų koncentravimas ir buferio keitimas - Ląstelių kultūrų skaidrinimas Techninės charakteristikos: - Srauto greitis: 12–120 l/min - Siurblio tipas: rotacinis mentinis siurblys Lodpfx Ajxxx Inspnjhn - Filtracijos formatas: kasetės ir pluoštinės membranos (galima konversija) - Valdymo sistema: UNICORN programinė įranga (atitinka FDA 21 CFR Part 11 reikalavimus)

Būklė: naujas, Gamybos metai: 2020, Funkcionalumas: visiškai funkcionalus, bakelio talpa: 30 000 l, Įranga: dokumentacija / vadovas, BRINOX 30,000 L WWAS / Solution Tank – 316L – PED – FAT – Complete GMP Documentation – incl. Saddle Support – 2020 – Mint Condition Manufacturer: BRINOX d.o.o. Tag No.: LV6456-BH1001 Serial No.: 1003464 Year of Manufacture: 2020 Condition: As new / unused Location: Europe LV6456-BH1001 Package 66 TECHNICAL DATA Product type: WWAS / solution tank / pharmaceutical process vessel Lodpfjykngfsx Apnshn Working volume: 30,000 litres Total volume: 33,213 litres Product-contact material: Stainless steel 1.4404 (AISI 316L) Surface finish: Chemically pickled, passivated and cleaned Surface roughness: Ra < 1.6 µm Standards and regulations: • PED 2014/68/EU compliant • CE marking present • Pharmaceutical design compliant with GMP Pressure data: Min.: –0.14 bar(g) Max.: +0.5 bar(g) Test pressure: 0.72 bar(g) Temperature range: –20 °C to +50 °C Hydrostatic pressure test performed. FAT – Factory Acceptance Test Comprehensively documented FAT conducted, including: • Dimensional, visual, and identification check • Weld seam and NDT inspections • Pressure test in accordance with PED • Inspection of all connections • Documentation and quality check FAT fully passed. FAT report available. DESIGN / CONSTRUCTION • Horizontal pharmaceutical process tank • Stainless steel 316L, pharmaceutical grade • Internal surfaces pickled and passivated • Hygienic, GMP-compliant construction Connections include: • Manway DN500 • Inlet DN100 • Outlet DN50 • Measurement, safety, and process ports Mechanical features: • Original BRINOX stainless steel saddle support included • Heavy-duty design • Lifting points for crane handling available CONDITION • Absolutely as new • Never installed or put into operation • Never filled with product • No corrosion or signs of use • Original industrial packaging present • Immediately available Saddle support also as new and included in the scope of supply. DOCUMENTATION – fully available (GMP-compliant) Extensive manufacturer and project documentation, incl.: • EU Declaration of Conformity and CE documentation • PED documents • Material certificates EN 10204 – 3.1 • Welding documentation (WPS / WPQR, welder lists) • NDT inspection reports • FAT protocol and pressure test report • Roughness and surface reports • Calibration certificates • Part drawings and parts lists • Operating and maintenance manuals Documentation fully available in digital format. TRANSPORT AND PACKAGING • Professional export packaging available • Original industrial packaging • Crane handling possible without issues • Worldwide shipping possible SUITABLE FOR • Pharmaceutical industry • Biotechnology • WWAS, WFI and PW systems • Sterile process solutions • GMP production facilities SPECIAL FEATURE Project surplus from an international pharmaceutical greenfield project with comprehensive FAT, PED compliance and GMP documentation. Large-volume BRINOX 30,000 L pharma process tank in new plant quality incl. saddle support – immediately available.

Būklė: naujas, Gamybos metai: 2020, Funkcionalumas: visiškai funkcionalus, mašinos/transporto priemonės numeris: BH6723-BH1001, bakelio talpa: 1 000 l, Įranga: dokumentacija / vadovas, BRINOX 1,000 L Pre-Charging Tank – 1.4435 – Double Jacket – PED Cat. IV Module G – TÜV – FAT – 2020 – As New Manufacturer: BRINOX d.o.o. Type: SVMMBI-1000 Tag No.: BH6723-BH1001 Serial Number: 1003454 Year of Manufacture: 2020 CE Marking: CE 0036 Condition: As new / unused TECHNICAL DATA Product type: Pre-charging / Process vessel Nominal volume: 1,000 L Total volume: 1,400 L Empty weight: approx. 610–762 kg Product contact material: 1.4435 (AISI 316L) Permissible pressure PS: -1 / +3 bar Test pressure PT: 5.4 bar Permissible temperature TS: -10 / +150 °C Fluid group: 1 Design according to AD 2000 Pressure vessel according to PED 2014/68/EU Category IV Module G – Single unit inspection Lsdeykqmzspfx Apnjhn Notified body: TÜV SÜD ID number: 0036 TÜV CERTIFICATION EU Declaration of Conformity (Module G) Certificate no.: Z-EU-SI-LJU-20-05-2702107-19125214 Inspection report no.: P-EU-SI-LJU-20-05-2702107-19125214 Final inspection carried out according to PED Annex I No. 3.2 Pressure test carried out according to Annex I No. 3.2.2 Acceptance without deviations Permissible number of load cycles: 10,000 (1.3 bar) Acceptance date: 20.05.2020 FAT – Factory Acceptance Test Full FAT performed in the factory: • Pressure test • Visual weld seam inspection • NDT inspections (RT/PT) • Dimensional check • Surface roughness measurement (≤ 0.8 µm) • Calibration test • Documentation review FAT completely documented. EXECUTION • Cylindrical, horizontal pressure vessel • Double jacket for heating/cooling • Internal surface electropolished • Pharmaceutical grade weld execution • Manway DN 500 • CIP connection • Safety valve • Pressure gauge • Multiple process and instrumentation nozzles • Suitable for pressure and vacuum operation CONDITION • Never used in production • Factory tested • TÜV Module G approved • Industrial mint condition • No signs of use • Immediately available DOCUMENTATION Complete, structured documentation available, including: • EU Declaration of Conformity • TÜV certificate with acceptance report • TÜV design review • FAT protocols • Material certificates EN 10204 3.1 • WPS/WPQR and welder lists • NDT reports • Surface roughness reports • Internal pressure test • Dimensional protocols • Calibration certificates • Parts list and drawings • Operating and maintenance manuals Digital documentation portfolio available. • Pharmaceutical solutions • WFI / PW systems • Buffer and media preparation • Sterile liquid processes • GMP plants • Biotechnology High-quality BRINOX pharmaceutical execution with PED Cat. IV Module G single unit test by TÜV SÜD (CE 0036) and complete FAT documentation. Not a standard tank – verified project quality. Immediately available.

Gamybos metai: 2015, būklė: labai geros būklės (naudotas), Allegedly very little used automatic filling line Plümat model BFL 851 for filling and sealing pre-sterilized IV-bags under pharmaceutical conditions. The unit consists of a safety frame, manual bag loading station, printing station, bag preparation station, tube cutting station, filling station, tube welding station, tube cooling station, and control panel. The filling line is a linear system compliant with GMP and FDA standards. - Bag formats (2 tubes = one loose tube, 30 mm in length, sealed with a vial stopper, and one 40 mm tube, welded or open): 100 ml, 250 ml, and 500 ml - Filling capacity: 100 ml / 250 ml / 500 ml = 600 bags/hour - Filling accuracy: 100 ml = ± 2.0%, 250 ml = ± 1.0%, 500 ml = ± 0.7% - Dosing range: 100 ml - 1000 ml - Sealing method used: Thermal welding - Filling system: Siemens S7 with flow measurement system and pneumatic filling valve - Controls: Siemens S7 MicroBox with Profibus DP and TP 1500 touch screen display - Power supply: 5.5 kW, 230/380 V, 50 Hz - Compressed air supply: approx. 700 l/min, min. 6 - max. 8 bar Lodpfx Apelhqndenehn - Cooling water supply: approx. 4 l/min, temperature 18-21 °C - Weight: approx. 1,350 kg (net) and 1,750 kg (gross) - Dimensions: 4,263 (length) x 1,050 (width) x 2,140 (height) mm

Būklė: naudotas, Gamybos metai: 2014, Gamintojas: MCPI Fine dosing Modelis: OPTI-FEEDER FD - SPA - klasė 2A Metai: 2014 Tipas: mikrodozavimo mašina / precizinio dozavimo įrenginys Produktų tipas: milteliai / granulės, sausa forma Dozavimo tipas: svorio pagal partiją gravimetriniu režimu Svorio matavimo grandinė: svarstyklės / precizinis svėrimo įrenginys Talpykla: 2 litrai Dozatoriaus talpyklos užpildymas: rankinis Elektroninis svėrimo valdymas ir stebėsena Ištraukimo angos skerspjūvis: 80 mm Dozavimo seka: 3 dozavimo greičiai (stambus, vidutinis ir smulkus), siekiant optimizuoti tikslumo / dozavimo greičio santykį Dozavimo kokybės kontrolė (+ ir - tolerancijos intervalas) Svarstyklių matavimo skiriamoji geba: 10 mg (0,01 g) Mažiausia dozė (apytiksliai): 250 mg Didžiausia dozė (apytiksliai): 500 g Atmintis iki 800 skirtingų dozavimo receptų Paleidimas: rankinis jutiklis Rezultatai išgaunami į USB raktą, analizuojami Excel programoje Valdymo blokas: įrenginys atitinka CE reikalavimus. Visi valdymo ir kontrolės elementai integruoti į šią dėžę (valdiklis, PLC, pavaros, saugos įtaisai, jungikliai ir kt.). Maitinimas: 220 V, vienfazis Dozatorius / valdymo dėžė: tiesioginis sujungimas Sudėtinių medžiagų sąlyčio dalys: 304L elektro-poliruotas nerūdijantis plienas Pagaminta pagal GMP reikalavimus Rankinis elektrinis atsuktuvas Ljdpfsx R Df Ssx Apnehn Mašinos matmenys: 95 x 75 x H 170 cm Yra dokumentacija

Gamybos metai: 2016, būklė: beveik kaip naujas (naudotas), Anton Paar MCP 150 Polarimeter – Gebraucht, Hervorragender Zustand Dieses Anton Paar MCP 150 Polarimeter wird in hervorragendem Zustand aus einem gut gepflegten, GMP-konformen Labor angeboten. Ideal für Labore, die präzise Messungen der optischen Drehung und vollständige 21 CFR Part 11-Konformität benötigen – besonders geeignet für Anwendungen in der Pharma-, Duftstoff- und Lebensmittel-Qualitätskontrolle. Hauptmerkmale: - Modell: MCP 150 - Wellenlänge: 589 nm (LED) - Messbereich: ±89,9°, Auflösung 0,001°, Genauigkeit ±0,01°, Wiederholbarkeit ±0,01° - Peltier-Temperaturregelung (15–35 °C) mit einer Genauigkeit von ±0,1 °C - Kompaktes Design: 370 × 320 × 130 mm, 8,6 kg - Schnittstellen: USB, Ethernet, RS232, CAN-Bus Ledpfx Aswbhktopnshn - Konform mit: 21 CFR Part 11, Ph. Eur., USP, JP, GAMP5, GMP Mitgeliefertes Zubehör: - Quarz-Kontrollplatte (+8°Z, +3°OR) mit Toolmaster™-Wireless-ID - 100 mm Edelstahl-Polarimetrieröhre mit Luer-Adapter und Peltier-Temperaturregelung - USB-Dongle für Anton Paar PS-Softwarelizenz - Vollständige Originaldokumentation, inklusive: - Installationsqualifizierung (IQ) - Kalibrierzertifikate - Bedienungsanleitung (Deutsch) Zustand: Gebraucht, aber in einwandfreiem, voll funktionsfähigem Zustand. Gerät und Zubehör sind sauber, gepflegt und betriebsbereit. Direkt aus einem kontrollierten GMP-Umfeld. Standort: Liestal, Schweiz. Für Preisangebot, Versand oder Besichtigung bitte kontaktieren.

Būklė: naudotas, Šiame skelbime siūlomas „Envair Technology B102“ mikrobiologinės saugos kabinetas su mobiliu stovu Įrenginys yra visiškai veikiantis ir paruoštas nedelsiant naudoti Apžvalga: „Envair Technology Bio 2 Essential“ (B102 serija) Sertifikatai ir paskirtis Visiškai atitinka BS EN 12469:2000 reikalavimus, užtikrinančius patikimus biologinės saugos standartus. Tinka darbui su biologiniais veiksniais iki ACDP 3-čios rizikos grupės (esant tinkamai laboratorijos vietai). Idealiai tinka ląstelių kultūroms ir susijusiems darbams. Konstrukcija ir dizainas Plotis: 1200 mm. Išorinis korpusas – dengtas baltu poliesteriu, pagamintas iš anglinio plieno. Darbo zona – išklota 304 klasės nerūdijančiu plienu su šoniniais stiklo intarpais. Darbo paviršius – nuimamas, gilintas, pagamintas iš 316 klasės nerūdijančio plieno. Oro srautas ir filtravimas Galimos recirkuliacinės arba ortakinės konfigūracijos. Įdiegta HEPA filtracija (H-14 klasė, ≥ 99.995% efektyvumas) pagal EN 1822‑1 standartą. Apšvietimas ir ventiliatoriai Apšviestas energiją taupančiais LED šviestuvais, įrengtais už darbo zonos ribų. Vėdinimui naudojami nepriklausomi EC tipo energiją taupantys ventiliatoriai, įrengti virš ir po darbo zona. Valdymo sąsaja Lhodpjxhfpkjfx Apnsn Integruotas membraninis valdymo pultas su lietimui jautriais mygtukais, sumontuotas virš darbo zonos, su animuota grįžtamojo ryšio indikacija. Atitiktis standartams Papildomai prie BS EN 12469:2000 ir HEPA filtrų standartų, „Bio 2 Essential“ spintos taip pat atitinka: IEC 61010‑1:2010 Oro kokybės standartai: ISO 5 klasė (BS EN ISO 14644‑1:2015) ir ES GMP A klasė.

Būklė: naudotas, Gamybos metai: 2011, Funkcionalumas: visiškai funkcionalus, mašinos/transporto priemonės numeris: L3B031, IMA MISTRAL Y 16 Bottle/Can Air Rinsing Machine – Used, Immediately Available Machine Data: Model: IMA MISTRAL Y 16 Type: Automatic Bottle/Can Air Rinsing and Extraction Machine Serial Number: L3B031 Year of Manufacture: 2011/2012 Manufacturer: IMA S.p.A. / IMA Swiftpack (Italy) Electrical Specification: 220/380 V, 3-phase, 50 Hz Space Requirement: approx. 400 × 140 × 220 cm Description & Special Features: This rotary air rinsing machine is designed for pharmaceutical and medical applications and is suitable for GMP-compliant internal cleaning of stable, round glass or plastic bottles using sterile compressed air. - Fully automatic bottle cleaning and extraction - Processes up to 200 containers/minute - Includes format sets for plastic bottles Ø 44 mm × height 95 mm - Additional format sets included: Ø 40 × 55 mm, Ø 60 × 130 mm Functionality: Bottles are fed in single file via a conveyor belt and screw, separated, transferred into a carousel, gripped, rotated 180°, and cleaned internally with nozzles (blow-out) and suction heads (extraction). The bottles are then transferred to the conveyor and the downstream machine. - Suitable for plastic and glass bottles and cans - High degree of automation, GMP-compliant design Documentation & Records: - Operating manuals (German, English, Italian) - Electrical diagrams - Layout drawings / guards layout - Spare parts catalogue - Blowing diagram / electrical diagram - FAT and SAT documents - Machine and operator’s manual in German Lhsdpfx Apow Sfa Ejnjn Scope of Delivery: - Complete machine - Spare parts as per catalogue - All original documentation (PDFs and hard copies) - Change parts for various bottle sizes Condition: - Used, from pharmaceutical production - Ready for immediate operation after installation - Immediately available Location: Çorlu, Turkey Price: On request

Būklė: naujas, Gamybos metai: 2020, Funkcionalumas: visiškai funkcionalus, mašinos/transporto priemonės numeris: BH6721-BH1001, bakelio talpa: 1 000 l, Įranga: dokumentacija / vadovas, BRINOX 1,000 L Pre-Filling Vessel – 1.4435 – Double Jacket – PED Module G – TÜV SÜD – FAT – 2020 – As New Lsdpfsykpqrox Apnjhn Manufacturer: BRINOX d.o.o. Type: SVMBBl-1000 Tag No.: BH6721-BH1001 Serial Number: 1003453 Year of Manufacture: 2020 Condition: As new / unused TECHNICAL DATA Product type: Pre-filling vessel / process vessel Nominal volume: 1,000 litres Total volume: 1,400 litres Empty weight: 762 kg Product-contact material: 1.4435 (AISI 316L pharmaceutical grade) CE marking: CE 0036 Permissible pressure PS: -1 / +3 bar Test pressure PT: 5.4 bar Permissible temperature TS: -10 °C to +150 °C Fluid group: 1 Design in accordance with AD 2000 regulations Pressure vessel according to PED 2014/68/EU Category IV Module G – individual inspection Notified body: TÜV SÜD Industrie Service GmbH (identification no. 0036) TÜV approval including final inspection and pressure test fully documented. FAT – Factory Acceptance Test The vessel was fully FAT-tested and released at the factory. Tests performed include: • Pressure test according to PED • Visual inspection of all weld seams • Non-destructive tests (RT, PT as per test plan) • Dimensional and drawing check (as-built) • Internal surface roughness measurement (Ra ≤ 0.8 µm) • Calibration test of manometers • Verification of labelling • Complete documentation audit FAT protocols fully available. DESIGN • Cylindrical, horizontal vessel • Double jacket for heating/cooling • Internally electropolished and passivated • High-gloss polished product surface • Pharmaceutical-grade weld seams • DN 500 manhole • CIP connections • Safety valve • Manometer • Bottom diaphragm valve • Agitator connection (DN 200) • Multiple spare connections • Heavy-duty trunnion / journal bearings • Transport and lifting equipment DOCUMENTATION – comprehensive and well-structured Extensive project-related quality and manufacturing documentation available, including: • EU declaration of conformity and warranty certificates • TÜV certificate with acceptance report (Module G) • TÜV design review and certification • 3.1 Material certificates • Welder lists and welding procedure qualifications (WPQR/WPS) • Non-destructive test reports (RT, PT etc.) • Analysis certificates for welding filler materials and shielding gas • Company qualification certificate • Surface roughness protocol • Surface treatment report • Dimensional accuracy inspection report • Internal pressure test report • Calibration certificates for manometers • Reports and EU conformity for installed components • Compilation with parts list • Component drawings • Operating and maintenance manuals Complete digital documentation folder available. CONDITION • Never in productive use • Stock item • Internal surface absolutely as new • No corrosion • No signs of use • Factory-new condition • Immediately available SUITABLE FOR • Pharmaceutical solutions • WFI / PW systems • Buffer and media preparation • Sterile liquid processes • GMP production facilities • Biotechnological applications FEATURES Premium BRINOX pharmaceutical-grade manufacturing with complete PED Module G individual inspection by TÜV SÜD, CE 0036 marking, and fully documented FAT testing. Not a standard tank – but project-quality, fully certified to GMP standards with comprehensive documentation. Available immediately.

Būklė: naudotas, vairuotojo kabina: kitas, pavaros tipas: kitas,

Būklė: naudotas, Gamybos metai: 2006, Funkcionalumas: visiškai funkcionalus, UHLMANN BLISTERLINIE Blisterlinie für die pharmazeutische Produktion in Reinräumen. Aus einem GMP-konformen Reinraumbetrieb und regelmäßig gewartet, vollautomatisch und modular aufgebaut, einfach in bestehende Produktionslinien integrierbar. Lieferung mit vollständiger technischer Dokumentation. Die Linie wurde für die interne Produktion stillgelegt. Bestehend aus: 1) UHLMANN BLISTERMASCHINE, MODELL UPS 4 Baujahr: 2006 PRODUKTIONSMERKMALE - Ausbringung: 15–50 Takte/Minute - Formbreite: 62–226 mm (min.–max.) - Blisterformat: min. 60 mm; max. 140×39 mm - Tiefen: PVC 12 mm; Alu 10 mm ENERGIEVERBRAUCH - Spannung: 3/N/PE AC 400 V - Strom: 30 A ABMESSUNGEN - Gewicht: 4.950 kg 2) UHLMANN KARTONIERMASCHINE, MODELL C2206 Baujahr: 2005 PRODUKTIONSMERKMALE - Max. Ausbringung: 200 Faltschachteln/Minute - Max. Schachtelgröße: 130 x 100 x 200 mm - Maximale Anzahl Blister: 10 - Verschlussarten: Steckverschluss, Heißleim - Geeignete Produkte: Blister, Flaschen ABMESSUNGEN - Gewicht: 6.000 kg ENERGIEVERBRAUCH - Spannung: 3/N/PE AC 400 V - Strom: 15 A 3) INOVA ETIKETTIERMASCHINE, MODELL EKK 62 Baujahr: 2006 ENERGIEVERBRAUCH - Spannung: 230/400 V - Frequenz: 50 Hz - Stromaufnahme: 9 A 4) INOVA MONTAGE- UND AUSSTOSSEINHEIT, MODELLE VSM1221 + TD210 Baujahr: 2006 ENERGIEVERBRAUCH (beide Maschinen) - Spannung: 230/400 V - Stromaufnahme: 5 A 5) BAUSCH + STRÖBEL SCHACHTELAUFRICHTER, MODELL ESS1001 Baujahr: 2013 PRODUKTIONSMERKMALE - Max. Ausbringung: 12.000 St./Std. - Etikettenlänge: 20 mm - 120 mm - Etikettenhöhe: 15 mm - 80 mm ABMESSUNGEN - Gewicht: 900 kg 6) HAPA INKJET-DRUCKER, MODELL H-230 Baujahr: 2005 PRODUKTIONSMERKMALE - Max. Takte: 120 Zyklen/Minute - Max. Druckgeschwindigkeit: 21,6 m/min - Druckkopf-Auflösung: 360 dpi - Bandbreite (min.–max.): 64–310 mm - Einzugs-/Drucklänge (min.–max.): 30–180 mm 7) SORTIMAT BLISTERHANDLING, MODELL CL400 VTS Baujahr: 2016 ABMESSUNGEN - Gewicht: 2.340 kg Lodpfezbhnwex Apnshn ENERGIEVERBRAUCH - Leistung: 3,4 kW / 5,0 A 8) UHLMANN BÜNDELUNGSMASCHINE, MODELL E 3060 Baujahr: 2006 PRODUKTIONSMERKMALE - Ausbringung: 60 Bündel - Kartongröße: max. 130 x 105 x 250 mm - Bündelgröße: max. 250 x 150 x 250 mm - Einlaufkapazität: 500 Kartons ABMESSUNGEN - Größe: ca. 1.400 x 2.000 x 4.300 mm - Gewicht: 2.100 kg ENERGIEVERBRAUCH - Spannung: 3/N/PE AC 400 V - Strom: 18 A 9) OPTIMA SPRITZENDOSIERER, MODELL SH120 Baujahr: 2008

Būklė: naujas, Gamybos metai: 2020, Funkcionalumas: visiškai funkcionalus, bakelio talpa: 9 000 l, Įranga: dokumentacija / vadovas, BRINOX 9,000 L Wash Solution Tank – 316L – Double Jacket – TÜV / PED – As New Manufacturer: BRINOX d.o.o. Tag No.: BH6751-BH1001 Package 31 Year of Manufacture: 2020 Condition: As new / unused Technical Specifications Product Type: Wash Solution Tank Nominal Capacity: approx. 9,000 liters Product-contacting Material: 1.4404 (AISI 316L) Design: Horizontal configuration CE Marking: Present Pressure Vessel according to PED 2014/68/EU TÜV inspected with acceptance report Double jacket available for heating/cooling Designed for pharmaceutical applications Internal Surface: • High-gloss polished • Pharmaceutical-grade weld seams • Documented surface quality Design / Equipment • Heavy-duty, project-specific fabrication in 316L stainless steel • Large-diameter manway with pressure lock • Integrated CIP spray lances / cleaning pipes • Multiple clamp and flange connections • Instrument connections (pressure, temperature, sensing) • Robust lifting and handling lugs • Industrial-grade heavy-duty construction • Externally pre-installed piping and process connections • Excellent accessibility for maintenance and inspection The images clearly show the high-quality workmanship, clean welding, and mirror-polished product-contacting internal surfaces. Condition • Never used in production • Stock item from project surplus • Absolutely clean interior • No corrosion • No signs of use • In as-new industrial condition • Immediately available Suitable for • Wash solutions in pharmaceutical processes • WFI / PW applications • CIP media • Buffer and process solutions • Biotechnology • GMP production facilities • Sterile liquid processes Documentation – complete and structured A comprehensive project-related quality and fabrication documentation is available for the tank, including: • EU Declaration of Conformity and warranty certificates • Reports and EU component documentation • Assembly documents • Partial drawings • TÜV certificate with acceptance report • Nameplate documentation • TÜV design validation and certification • Welder lists, welding procedure qualifications, work samples • Analysis certificates for welding consumables • Analysis certificates for shielding gas • Manufacturer qualification certificate • Non-destructive testing (NDT) reports • Material certificates (3.1) • Calibration certificates • Internal pressure test report • Dimensional accuracy inspection • Roughness protocol • Surface treatment report • Operating and maintenance manuals (device) • Operating and maintenance manuals (components) Ljdpfjykkivsx Apnehn • FAT documents (Factory Acceptance Test) Complete documentation portfolio available digitally. Special Features This is not a standard tank, but a high-end project-specific fabrication in genuine pharmaceutical quality with certified pressure design, documented manufacturing, and full PED compliance with TÜV approval. Heavy, robust construction, large-dimensioned connections, and CIP integration make this tank ideal for demanding GMP applications.

Būklė: naujas, Gamybos metai: 2020, Funkcionalumas: visiškai funkcionalus, bakelio talpa: 3 500 l, Įranga: dokumentacija / vadovas, BRINOX 3,500 L Batch Tank – 1.4435 – Double Jacket – PED Module G – TÜV SÜD – FAT – 2020 – As New Manufacturer: BRINOX d.o.o. Type: SVMBHI-3500 Tag No.: BH6770-BH1001 Serial No.: 1003460 Year of manufacture: 2020 Condition: As new / unused Package: BH6770-BH1001 Package 28 TECHNICAL DATA Product type: Batch tank / Pressure vessel Working volume: 3,500 litres Total volume: 4,304 litres Jacket volume: 202 litres Empty weight: 1,958 kg Product contact material: 1.4435 Jacket: 1.4404 Lodjylng Uspfx Apnehn CE Marking: CE 0036 Design pressure vessel PS: -1 / +3 bar Test pressure vessel PT: 5.6 bar Design pressure jacket PS: -1 / +6 bar Test pressure jacket PT: 10.8 bar Design temperature TS: -10 °C to +150 °C Fluid group: 2 Design according to AD 2000 regulations Pressure vessel according to PED 2014/68/EU Category III Module G – Individual Inspection Notified body: TÜV SÜD Industrie Service GmbH (ID No. 0036) TÜV approval including final inspection and pressure test fully documented. FAT – Factory Acceptance Test The vessel underwent full FAT testing and approval at the manufacturer’s site. Inspections performed include: • Pressure test in accordance with PED • Visual inspection of all weld seams • Non-destructive testing (RT, PT as per inspection plan) • Dimensional and drawing check (as-built) • Internal surface roughness measurement (Ra ≤ 0.8 µm) • Calibration testing of manometers • Verification of markings • Complete documentation review Full FAT protocols available. DESIGN FEATURES • Cylindrical, horizontal tank • Double jacket with half-pipe coil system • Internally electropolished and passivated • Mirror-finish product surface • Pharmaceutical-grade welds • Manway DN 500 • Powder / product inlet DN 300 • CIP connections • Safety valve • Pressure and temperature ports • Agitator port • Heavy-duty trunnion mounts • Lifting lugs DOCUMENTATION – complete and structured Comprehensive, project-related quality and manufacturing documentation, including: • EU Declaration of Conformity and warranty certificates • TÜV certificate with inspection report (Module G) • TÜV design assessment and certification • 3.1 material certificates • Welder lists and welding procedure qualifications (WPQR/WPS) • Non-destructive testing reports (RT, PT etc.) • Analysis certificates for welding consumables and shielding gases • Company qualification certificate • Surface roughness protocol • Surface treatment report • Dimensional accuracy report • Internal pressure test report • Calibration certificates • Component conformity and documentation as per EU • Parts list assemblies • Component drawings • Operation and maintenance manuals Complete digital documentation folder available. CONDITION • Never used in production • Stock item • Interior surface absolutely as-new • No corrosion • No signs of use • Industry-new condition • Immediately available SUITABLE FOR • Pharmaceutical solutions • WFI / PW systems • Buffer and media preparation • Sterile liquid processes • GMP production facilities • Biotechnological applications SPECIAL FEATURES Premium BRINOX pharmaceutical manufacture with full PED Module G individual approval by TÜV SÜD, CE 0036 marking, and documented FAT testing. Not a standard tank – this is certified project quality with comprehensive GMP-compliant documentation.

Būklė: naudotas, Gamybos metai: 2014, Hersteller: MCPI Fine Dosing Modell: OPTI-FEEDER FD - SPA - Klasse 2A Baujahr: 2014 Typ: Mikro-Dosieranlage / Präzisionsdosiergerät Produktart: Pulver / Granulate, trocken Dosierart: Chargenweise Dosierung nach Gewicht im gravimetrischen Modus Wiegekette: Präzisionswaage / Präzisionswägezelle Befüllung des Dosierbehälters: Manuell Elektronische Wäge- und Steuerungseinheit Austrittsquerschnitt des Dosierförderers: 80 mm Dosierablauf: 3 Dosiergeschwindigkeiten (grob, mittel und fein) zur Optimierung des Verhältnisses zwischen Genauigkeit und Dosiergeschwindigkeit Überwachung der Dosierqualität (Toleranzbereich +/-) Waagenauflösung: 10 mg (0,01 g) Lhjdpfjx R Dh Hex Apnen Mindestdosierung (geschätzt): 250 mg Höchstdosierung (geschätzt): 500 g Speicher für 800 verschiedene Dosierrezepturen Auslösung: Fußpedal Auswertung der Ergebnisse über USB-Stick, Analyse in Excel möglich. Steuereinheit: Schaltschrank nach CE-Norm. Alle Steuerungs- und Bedienelemente sind in diesem Schrank integriert (Controller, SPS, Frequenzumrichter, Sicherheitseinrichtungen, Schalter etc.). Stromversorgung: 220V – einphasig Verbindung Dosierer / Steuerung: direkt Produktberührende Teile: Edelstahl 304L, elektropoliert. Fertigung gemäß GMP-Richtlinien Maschinenabmessungen: 95 x 75 x H 170 cm Dokumentation vorhanden

Būklė: naudotas, Angeboten werden 8 Envair Mobile Isolatoren verschiedener Spezifikationen, aktuell bei uns am Lager verfügbar. Die Geräte befinden sich in einem voll funktionsfähigen Zustand und sind sofort einsatzbereit. Envair Mobile Isolator Envair Technology ist ein britischer Hersteller, der sich auf Reinluft- und Containment-Lösungen für die Gesundheits-, Biotechnologie- und Pharmaindustrie spezialisiert hat. Die Produktpalette umfasst zahlreiche Isolatoren, die kontrollierte Umgebungen für den Umgang mit Gefahrstoffen bieten und sowohl den Bediener- als auch Produktschutz garantieren. Anwendungsbereiche - Krankenhausapotheken: Zur Herstellung von TPN (Totale parenterale Ernährung), CIVAS und aseptischer Herstellung. - Pharmazeutische Labore: Handhabung von HPAPI (hochwirksame pharmazeutische Wirkstoffe) und steriler Herstellung. - Sterilitätstests: Sichere, kontrollierte Umgebung zur Produktprüfung. - F&E-Einrichtungen: Sicheres Containment während experimenteller Entwicklungen oder frühen Entwicklungsphasen. Wichtige Merkmale der Envair-Isolatoren - Modelle mit Über- und Unterdruck erhältlich: Überdruck-Isolatoren schützen das Produkt vor Kontamination; Unterdruck-Isolatoren schützen das Bedienpersonal vor gefährlichen Stoffen. - GMP-konform: Viele Envair-Isolatoren erfüllen die Anforderungen der EU-GMP Klasse A und ISO 5 und garantieren eine sterile, kontrollierte Umgebung. - Individuelle Ausführungen: Envair bietet maßgeschneiderte Lösungen entsprechend den Anforderungen des Kunden, inklusive spezieller Abmessungen und technischer Ausstattung. - Fortschrittliche Containment-Technologie: Ausgestattet mit automatisierten Dichtigkeitsprüfungen (pressure decay), elektromagnetisch verriegelten Übergabekammern und integrierten Dekontaminationssystemen. - Benutzerfreundliche Steuerung: Die meisten Geräte verfügen über intuitive Touchscreen-Bedienung und speicherprogrammierbare Steuerungen (SPS/PLC) für einfache und effiziente Bedienung. Wachsende Anforderungen an Containment bei HPAPI Lsdpfxsxv Dhbe Apnshn Die Nachfrage nach personalisierten Arzneimitteln mit hochwirksamen pharmazeutischen Wirkstoffen (HPAPI), besonders bei modernen onkologischen, kardiovaskulären und Diabetes-Therapien, steigt rapide an. Solche Präparate erfordern oftmals kurze Durchlaufzeiten, weshalb Prozesshersteller flexible, schnelle Workflows entwickeln müssen. Gerade in diesen Hochrisiko- und Hochwert-Umgebungen ist eine GMP-gerechte Arbeitsumgebung nicht optional, sondern zwingend erforderlich. Dabei wird oft übersehen, dass die Menschen, die diese komplexen Wirkstoffe entwickeln, herstellen und abgeben, einem erheblichen Expositionsrisiko gegenüber teils lebensgefährlichen Substanzen ausgesetzt sind. Ihr Schutz hat höchste Priorität, um eine verlässliche Versorgung mit modernen Arzneimitteln sicherzustellen. Kompetenz im HPAPI-Handling für CMOs & CDMOs Envair verfügt über fundierte Erfahrung in der Unterstützung von Lohnherstellern (CMOs) und Lohnentwicklern (CDMOs) im sicheren Umgang mit HPAPI – auch in bestehenden nicht eingehausten Anlagen. Die Isolatorsysteme werden individuell geplant, hergestellt und installiert, um anspruchsvolle Containment-Anforderungen mit Expositionsgrenzwerten unter 1μg/m³ (OEB 5) zu erfüllen. Jedes System wird exakt auf den jeweiligen Standort und Prozessschritt ausgelegt, z. B. für das Wägen, Mischen, Mahlen, Sprühtrocknen oder Verpacken. Anwendungsbereiche (erneut) - Krankenhausapotheken: Zubereitung von TPN, CIVAS und aseptischer Verteilung. - Pharmaz