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MCSL30S01

Millidisk® 30 Cartridge Media: Durapore® 5.0 µm

Chemistry: Hydrophilic Polyvinylidene Fluoride (PVDF)

Synonym(s):

Millidisk Cartridge 30-stack 5.0 μm Hydrophilic, Durapore® 5.0 µm, Millidisk® Cartridge

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About This Item

eCl@ss:
32031690
UNSPSC Code:
23151806
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Product Name

Millidisk® 30 Cartridge Media: Durapore® 5.0 µm, Chemistry: Hydrophilic Polyvinylidene Fluoride (PVDF)

Quality Segment

400

material

PVDF , polysulfone , polysulfone support, silicone seal

sterility

non-sterile

sterilization compatibility

autoclavable compatible
steam-in-place compatible

product line

Millidisk® 30

feature

hydrophilic

manufacturer/tradename

Millidisk®

parameter

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

technique(s)

prefiltration: suitable

filtration area

1500 cm2

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

≤7.5 mg/device

matrix

Durapore®

pore size

5.0 μm pore size

input

sample type liquid

bubble point

≥138 mbar (2 psig), air with water at 23 °C

cartridge code

not applicable

General description

Device Configuration: Cartridge
Stack Design: 30 Stak

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method
5 SIP cycles of 60 min @ 135 °C; 5 autoclave cycles of 60 min @ 126 °C
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: using sterilized device 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
MILLIDISK is a registered trademark of Merck KGaA, Darmstadt, Germany

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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