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MFGL02GH3 Non-sterilized Millipak® Final Fill 20 Filter Unit 0.22  µm 1/4  in. HB/HB

MFGL02GH3
3  Double Easy-Open bag
Purchase on Sigma-Aldrich

概述

Replacement Information
Description
Catalogue NumberMFGL02GH3
Trade Name
  • Millipak®
DescriptionNon-sterilized Millipak® Final Fill 20 Filter Unit 0.22  µm 1/4  in. HB/HB
References
Product Information
HS Code8421 29 90
Device ConfigurationCapsule
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®
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 ConnectionStepped Hose Barb
Outlet ConnectionStepped Hose 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 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
产品目录编号 GTIN
MFGL02GH3 04054839378263

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 C2SB36872
Millipak Final Fill Capsule Durapore Membrane C3KB52123
Millipak Final Fill Capsule Durapore Membrane C1EB92064
Millipak Final Fill Capsule Durapore Membrane C1JB35038
Millipak Final Fill Capsule Durapore Membrane C2BB17895
Millipak Final Fill Capsule Durapore Membrane C2HB31903
Millipak Final Fill Capsule Durapore Membrane C2KB31907
Millipak Final Fill Capsule Durapore Membrane C2SB59656
Millipak Final Fill Capsule Durapore Membrane C3MB56879
Millipak Final Fill Capsule Durapore Membrane C3NB56880
Show more

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

数据表

标题
Durapore® Family Guide

用户指南

标题
Wetting Instructions for Filter Units with Durapore Membrane

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