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MFGL06GL3 Non-sterilized Millipak® Final Fill 60 Filter Unit 0.22  µm 1 1/2  in. TC - 1/2 in. HB

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MFGL06GL3
3  Double Easy-Open bag
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Overview

Replacement Information
Description
Catalogue NumberMFGL06GL3
Trade Name
  • Millipak®
DescriptionNon-sterilized Millipak® Final Fill 60 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 Rate1.51 L/min @ 0.86   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 Area300 cm²
Process Volume60 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
Catalogue Number GTIN
MFGL06GL3 04054839379673

Documentation

Material Qualification Dossier

TitleVersion
3.0

Quality Management Dossier (Open Access)

Title

Operational Excellence Dossier

Title

Operational Excellence Dossier (Second Sterilization)

Title

Certificates of Quality

Title
Millipak Final Fill Capsule Durapore Membrane C2CB23877
Millipak Final Fill Capsule Durapore Membrane C4MB85373

Technical Info

Title
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

User Guides

Title
Wetting Instructions for Filter Units with Durapore Membrane

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