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MFGL10GL3 Non-sterilized Millipak® Final Fill 100 Filter Unit 0.22  µm 1 1/2  in. TC - 1/2  in. HB

MFGL10GL3
3  Double Easy-Open bag
Purchase on Sigma-Aldrich

概述

Replacement Information
Description
Catalogue NumberMFGL10GL3
Trade Name
  • Millipak®
DescriptionNon-sterilized Millipak® Final Fill 100 Filter Unit 0.22  µm 1 1/2  in. TC - 1/2  in. HB
References
Product Information
Device ConfigurationCapsule
Connections, Inlet/Outlet38  mm (1½  in.) sanitary flange inlet and 13  mm (½  in.) stepped hose barb outlet
Maximum Differential Pressure, bar (psid)Foward:80 psi (5.5 bar) at 25 °C (0.1 µm, 0.22 µm, 0.45 µm, hydrophobic 0.22 µm); Reverse: 10 psi (0.7 bar) at 25 °C
Maximum Inlet Pressure, bar (psi)80 psi (5.5 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®
Sterilitynon-sterilized
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 ConnectionStepped Hose Barb
Bubble Point at 23 °C≥ 50 psi (3450 mbar) air with water
Flow Rate3.81 L/min @ 1.1   bar ∆P
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 Area500 cm²
Process Volume100 L
Inlet Connection Diameter1 1/2 in.
Outlet Connection Diameter1/2 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
产品目录编号 GTIN
MFGL10GL3 04054839379697

Documentation

Material Qualification Dossier

标题版本
1.0

Quality Management Dossier (Open Access)

Title

Operational Excellence Dossier

Title

Operational Excellence Dossier (Second Sterilization)

Title

质量证书

标题
Millipak Final Fill Capsule Durapore Membrane C2NB26438
Millipak Final Fill Capsule Durapore Membrane C3HB29751
Millipak Final Fill Capsule Durapore Membrane C4AB80294
Millipak Final Fill Capsule Durapore Membrane C4DB17725
Millipak Final Fill Capsule Durapore Membrane C4EB09366
Millipak Final Fill Capsule Durapore membrane C3KB46421

技术信息

标题
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

用户指南

标题
Wetting Instructions for Filter Units with Durapore Membrane

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产品族

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