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MFGL06GT3

Millipak® Final Fill 60 Durapore®

Inlet: 1.5 in. Sanitary Flange Outlet: 1.5 in. Sanitary Flange Vent: 1/8 in. Hose Barb

Synonym(s):

Durapore® 0.22 µm, Millipak® Final Fill Capsule

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About This Item

UNSPSC Code:
23151806
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Product Name

Millipak® Final Fill 60 Durapore®, Inlet: 1.5 in. Sanitary Flange Outlet: 1.5 in. Sanitary Flange Vent: 1/8 in. Hose Barb

Quality Level

400

material

polysulfone device, polysulfone support

agency

meets EP 2.6.14, meets JP 4.01, meets USP 85

sterility

irradiated, non-sterile

sterilization compatibility

gamma compatible

product line

Millipak® Final Fill 60

feature

hydrophilic

manufacturer/tradename

Millipak®

parameter

1.51 L/min flow rate at 0.86 bar (ΔP), 10 psi max. differential pressure (0.7 bar) at 25 °C (Reverse), 5.5 bar max. inlet pressure (80 psi) at 25 °C, 60 L process volume, 80 psi max. differential pressure (5.5 bar) at 25 °C (Forward)

technique(s)

sterile filtration: suitable

L

4.3 in.

W

3.0 in.

filter filtration area

300 cm2

impurities

<0.25 EU/mL USP bacterial endotoxins (LAL test, per device; aqueous extraction), <0.25 EU/mL bacterial endotoxins (LAL test, per device; aqueous extraction)

matrix

Durapore®

pore size

0.22 μm pore size

bubble point

≥50 psi (3450 mbar), air with water

fitting

(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: 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.

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

Analysis Note

Bacterial Grow-Through: Quantitative retention of 1 x 107 CFU/cm2 Brevundimonas diminuta ATCC® 19146 per ASTM® F838 methodology.

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 general guidelines section of user guide shipped with this product
  • Storage Statement: Please refer user guide shipped with this product
  • Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations

These products are manufactured in a facility which is certified to ISO 9001:2015 Quality Management Systems.

Legal Information

ASTM is a registered trademark of American Society for Testing and Materials
ATCC is a registered trademark of American Type Culture Collection
Durapore is a registered trademark of Merck KGaA, Darmstadt, Germany
MILLIPAK is a registered trademark of Merck KGaA, Darmstadt, Germany

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Regulatory Information

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Global Trade Item Number

SKUGTIN
MFGL06GT304054839379888