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Attention: We have moved. Merck Millipore products are no longer available for purchase on MerckMillipore.com.

MFVL10GB3 MilliporeNon-sterilized Millipak^® Final Fill 100 Filter Unit 0.1 µm 1/2 in. HB/HB

Recommended Products

Áttekintés

Replacement Information

Description
Catalogue Number	MFVL10GB3
Trade Name	Millipak^®
Description	Non-sterilized Millipak^® Final Fill 100 Filter Unit 0.1 µm 1/2 in. HB/HB

References

Product Information
Device Configuration	Capsule
Connections, Inlet/Outlet	13 mm (½ in.) stepped hose barb inlet and 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	0.1 µm
Inlet Connection	Stepped Hose Barb
Outlet Connection	Stepped Hose Barb
Bubble Point at 23 °C	≥ 70 psi (4830 mbar) air with water
Flow Rate	1.31 L/min @ .86 bar ΔP
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	500 cm²
Process Volume	100 L
Inlet Connection Diameter	1/2 in.
Outlet Connection Diameter	1/2 in.

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
Katalógusszám	GTIN
MFVL10GB3	04054839378348

Documentation

Material Qualification Dossier

Title	Version
EMPROVE® Material Qualification Dossier - MFVL10GB3	1.0

Operational Excellence Dossier

Title
Non-sterilized Millipak® Final Fill 100 Filter Unit 0.1 µm 1/2 in. HB/HB

Operational Excellence Dossier (Second Sterilization)

Title
Non-sterilized Millipak® Final Fill 100 Filter Unit 0.1 µm 1/2 in. HB/HB

Certificates of Quality

Title
Millipak Final Fill Capsule Durapore Membrane C4HB50010

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

Kapcsolódó termékek és alkalmazások

Product Families

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