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MPHL20CL3

Millipak® 200 Capsule Media: Durapore® 0.45 µm

Chemistry: Hydrophilic Polyvinylidene Fluoride (PVDF) Inlet: 1-1/2 in. Sanitary Flange Outlet: 1-1/2 in. Sanitary Flange

Synonym(s):

Gamma Compatible Millipak -200 Filter Unit 0.45 μm 1-1/2 in. TC/TC, Durapore® 0.45 µm, Millipak® Capsule

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About This Item

UNSPSC Code:
23151806
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Product Name

Millipak® 200 Capsule Media: Durapore® 0.45 µm, Chemistry: Hydrophilic Polyvinylidene Fluoride (PVDF) Inlet: 1-1/2 in. Sanitary Flange Outlet: 1-1/2 in. Sanitary Flange

Quality Level

400

material

PVDF , PVDF vent cap, polycarbonate , polycarbonate support

sterility

irradiated, non-sterile

sterilization compatibility

gamma compatible

product line

Millipak® 200

feature

gamma compatible, hydrophilic

manufacturer/tradename

Millipak®

parameter

0.35 bar max. differential pressure (5 psid) at 123 °C (Forward), 0.7 bar max. differential pressure (10 psid) at 25 °C (Reverse), 1.7 bar max. differential pressure (25 psid) at 80 °C (Forward), 100 L process volume, 23 L/min flow rate at 2.1 bar (ΔP), 4.1 bar max. differential pressure (60 psid) at 25 °C (Forward), 5.2 bar max. inlet pressure (75 psi) at 25 °C

technique(s)

bioburden reduction: suitable

L

6.0 in.

W

3.0 in.

filtration area

1000 cm2

inlet connection diam.

1.5 in.

outlet connection diam.

1.5 in.

impurities

≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction), <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)

gravimetric extractables

≤5 mg/device

matrix

Durapore®

pore size

0.45 μm

bubble point

≥1790 mbar (26 psig), air with water at 23 °C

fitting

inlet sanitary flange, outlet sanitary flange, (38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)

General description

Device Configuration: Capsule

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method
3 autoclave cycles of 90 min @ 123°C; not in-line steam sterilizable
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).

Analysis Note

Gravimetric Extractables: after 24 hours in water at controlled room temperature
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥200 mL

Other Notes

Directions for Use

  • Organism Retention: Microorganism
  • Mode of Action: Filtration (size exclusion)
  • Application: BioProcessing
  • Intended Use: Reduction or removal of microorganism/bioburden
  • Instructions for Use: Please refer Wetting Instructions for Filter Units with Durapore® Membrane user guide
  • Storage Statement: Store in dry location
  • Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

Legal Information

Durapore is a registered trademark of Merck KGaA, Darmstadt, Germany
MILLIPAK is a registered trademark of Merck KGaA, Darmstadt, Germany

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Certificates of Analysis (COA)

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Global Trade Item Number

SKUGTIN
MPHL20CL304053252252952