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MFGL20GK3 MilliporeNon-sterilized Millipak^® Final Fill 200 Filter Unit 0.22 µm 3/4 in. TC - 1/2 in. HB

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Replacement Information

Description
Catalogue Number	MFGL20GK3
Trade Name	Millipak^®
Description	Non-sterilized Millipak^® Final Fill 200 Filter Unit 0.22 µm 3/4 in. TC - 1/2 in. HB

References

Product Information
Device Configuration	Capsule
Connections, Inlet/Outlet	19 mm (¾ in.) sanitary flange inlet and 13 mm (½ in.) 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 Practices	These products are manufactured in a facility which is certified to ISO® 9001:2015 Quality Management Systems.
Quality Level	MQ400

Applications

Biological Information
Bacterial Endotoxins	Aqueous 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.
Media	Durapore^®
Sterility	non-sterilized
Sterilization	Device 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 Retention	Quantitative retention of 10⁷CFU/cm² Brevundimonas diminuta ATCC^® 19146 per AST^® F838 methodology.
Wettability	Hydrophilic

Physicochemical Information
Pore Size	0.22 µm
Inlet Connection	Sanitary Flange
Outlet Connection	Hose Barb
Bubble Point at 23 °C	≥ 50 psi (3450 mbar) air with water
Flow Rate	7.61 L/min @ 1.1 bar ∆P
Non-Fiber Releasing	This 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 Endotoxins	Aqueous 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 Area	1000 cm²
Process Volume	200 L
Inlet Connection Diameter	3/4in.
Outlet Connection Diameter	1/2in.

Materials Information
Chemistry	Polyvinylidene Fluoride (PVDF)
Device Material	Polysulfone
Support Material	Polysulfone

Toxicological Information

Safety Information according to GHS

Safety Information

Product Usage Statements

Storage and Shipping Information

Packaging Information
Material Size	3
Material Package	Double Easy-Open bag

Transport Information

Supplemental Information

Specifications

Global Trade Item Number
Numero di catalogo	GTIN
MFGL20GK3	04054839379468

Documentation

Material Qualification Dossier

Titolo	Versione
EMPROVE® Material Qualification Dossier - MFGL20GK3	1.0

Quality Management Dossier (Open Access)

Title
Non-sterilized Millipak® Final Fill 200 Filter Unit 0.22 µm 3/4 in. TC - 1/2 in. HB

Operational Excellence Dossier

Title
Non-sterilized Millipak® Final Fill 200 Filter Unit 0.22 µm 3/4 in. TC - 1/2 in. HB

Operational Excellence Dossier (Second Sterilization)

Title
Non-sterilized Millipak® Final Fill 200 Filter Unit 0.22 µm 3/4 in. TC - 1/2 in. HB

Certificati di Qualità

Titolo
Millipak Final Fill Capsule Durapore Membrane C2CB93081
Millipak Final Fill Capsule Durapore Membrane C0SB63234
Millipak Final Fill Capsule Durapore Membrane C3MB64641
Millipak Final Fill Capsule Durapore Membrane C3PB67077
Millipak Final Fill Capsule Durapore Membrane- C3CB90997
Millipak Final Fill Capsule Durapore membrane C4AB69838
Millipak Final Fill Capsule Durapore membrane C4AB80295

Informazioni tecniche

Titolo
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

Scheda tecnica

Titolo
Durapore® Family Guide

Manuali d'uso

Titolo
Wetting Instructions for Filter Units with Durapore Membrane

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