Millipore Sigma Vibrant Logo
Attention: We have moved. Merck Millipore products are no longer available for purchase on MerckMillipore.com.Learn More

MFGL02SH3 Gamma sterilized Millipak® Final Fill 20 Filter Unit 0.22  µm 1/4  in. HB/HB

MFGL02SH3
3  Double Easy-Open bag
Purchase on Sigma-Aldrich

Overview

Replacement Information
Description
Catalogue NumberMFGL02SH3
Trade Name
  • Millipak®
DescriptionGamma sterilized Millipak® Final Fill 20 Filter Unit 0.22  µm 1/4  in. HB/HB
References
Product Information
HS Code8421 29 90
Device ConfigurationGamma Gold Capsule
Connections, Inlet/Outlet6  mm (¼  in.) stepped hose barb inlet and 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 ConnectionStepped Hose Barb
Outlet ConnectionStepped Hose Barb
Bubble Point at 23 °C≥ 50 psi (3450 mbar) air with water
Flow Rate0.51 L/min @ .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 Diameter1/4 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
Catalogue Number GTIN
MFGL02SH3 04054839378454

Documentation

Material Qualification Dossier

TitleVersion
1.0

Quality Management Dossier (Open Access)

Title

Operational Excellence Dossier

Title

Certificates of Quality

Title
Millipak Final Fill Capsule Durapore Membrane C1EB93050
Millipak Final Fill Capsule Durapore Membrane C3NB59536
Millipak Final Fill Capsule Durapore Membrane C4AB69836
Millipak Final Fill Capsule Durapore Membrane C2DB58019
Millipak Final Fill Capsule Durapore Membrane- C0EB71687
Millipak Final Fill Capsule Durapore membrane C3HB37507
Millipak Final Fill Capsule Durapore membrane C4AB69672

Technical Info

Title
Integrity Test Troubleshooting - Beyond Rewet and Retest
Reduce Contamination Risks and Simplify Filtration System Design and Operation

Data Sheet

Title
Durapore® Family Guide

User Guides

Title
Wetting Instructions for Filter Units with Durapore Membrane

Related Products & Applications

Product Families

Millipak® Final Fill Filters

Stacked disc filters designed to maximize recovery and enhance protection of your high value product
Learn More >>