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MFGL02SC3 Gamma sterilized Millipak® Final Fill 20 Filter Unit 0.22  µm 3/4  in. TC - 1/4   in. HB

MFGL02SC3
3  Double Easy-Open bag
Purchase on Sigma-Aldrich

Descripción

Replacement Information
Description
Catalogue NumberMFGL02SC3
Trade Name
  • Millipak®
DescriptionGamma sterilized Millipak® Final Fill 20 Filter Unit 0.22  µm 3/4  in. TC - 1/4   in. HB
References
Product Information
Device ConfigurationGamma Gold Capsule
Connections, Inlet/Outlet19  mm (¾  in.) sanitary flange inlet and 6  mm (¼  in.) hose barb outlet
Maximum Differential Pressure, bar (psid)Forward:60 psi (4.1 bar) at 25 °C; 50 psi(3.5 bar) at 25 °C; (5 µm) 25 psi (1.7 bar) at 80 °C; Reverse: 10 psi (0.7 bar) at 25 °C
Maximum Inlet Pressure, bar (psi)60 psi (4.1 bar) at 25 °C
Good Manufacturing PracticesThese products are manufactured in a facility which is certified to ISO® 9001:2015 Quality Management Systems.
Quality LevelMQ400
Applications
Biological Information
Bacterial EndotoxinsAqueous extraction contains < 0.25 EU/mL per device as determined using the Limulus Amebocyte Lysate (LAL) test, meeting requirements of USP <85>, EP 2.6.14 and JP 4.01.
MediaDurapore®
Sterilitysterilized by gamma irradiation
SterilizationDevice integrity and retention was maintained after 3 autoclave cycles of 90 minutes at 126  °C. Devices can withstand a dose ≤ 40  kGy gamma exposure.
Bacterial RetentionQuantitative retention of 107 CFU/cm2 Brevundimonas diminuta ATCC® 19146 per AST® F838 methodology.
WettabilityHydrophilic
Physicochemical Information
Pore Size0.22 µm
Inlet ConnectionSanitary Flange
Outlet ConnectionHose Barb
Bubble Point at 23 °C≥ 50 psi (3450 mbar) air with water
Flow Rate0.51 L/min @ 0.69 bar ΔP
Non-Fiber ReleasingThis product was manufactured with a Durapore® membrane which meets the criteria for a “non-fiber releasing” filter as defined in 21 CFR 210.3 (b)(6), validated based on large volume parenteral specifications as detailed in USP <788> Particulate Matter in Injections
USP Bacterial EndotoxinsAqueous extraction contains < 0.25 EU/mL per device as determined using the Limulus Amebocyte Lysate (LAL) test, meeting requirements of USP <85>, EP 2.6.14 and JP 4.01.
Dimensions
Filtration Area100 cm²
Process Volume20 L
Inlet Connection Diameter3/4 in.
Outlet Connection Diameter1/4 in.
Materials Information
Chemistry
  • Polyvinylidene Fluoride (PVDF)
Device Material
  • Polysulfone
Support MaterialPolysulfone
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Packaging Information
Material Size3
Material PackageDouble Easy-Open bag
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Número de referencia GTIN
MFGL02SC3 04054839378768

Documentation

Material Qualification Dossier

CargoVersión
1.0

Quality Management Dossier (Open Access)

Title

Operational Excellence Dossier

Title

Certificados de calidad

Cargo
Millipak Final Fill Capsule Durapore Membrane - C0EB52658
Millipak Final Fill Capsule Durapore Membrane C3PB67070
Millipak Final Fill Capsule Durapore membrane C3HB26330
Millipak Final Fill Capsule Durapore membrane C4CB93433

Licencias necesarias e Información técnica

Cargo
Improved Product Recovery using Blow-down and Millipak®Final Fill Filters
Integrity Test Troubleshooting - Beyond Rewet and Retest
Reduce Contamination Risks and Simplify Filtration System Design and Operation

Ficha técnica

Cargo
Durapore® Family Guide

Manuales del usuario

Cargo
Wetting Instructions for Filter Units with Durapore Membrane

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