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Merck

MPGL2GCA3

Millipore

Durapore® 0.22 µm, Millipak® Capsule

sterile

동의어(들):

Sterile Millipak-200 Filter Unit 0.22 m 9/16 in. HB/HB

로그인조직 및 계약 가격 보기


About This Item

UNSPSC 코드:
23151806

material

PVDF
PVDF vent cap
polycarbonate
polycarbonate support

Quality Level

무균

irradiated
sterile

제품 라인

EMPROVE® Filter

특징

hydrophilic

제조업체/상표

Millipak®

파라미터

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
19 L/min flow rate at 2.8 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

기술

sterile filtration: suitable

여과 면적

1000 cm2

입구 연결 직경

9/16 in.

출구 연결 직경

9/16 in.

불순물

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

중량 추출물

≤5 mg/device

기질

Durapore®

공극 크기

0.22 μm

버블 포인트(bubble point)

≥3450 mbar (50 psig), air with water at 23 °C

피팅

inlet hose barb
outlet hose barb
(14 mm (9/16 in.) Hose Barb Inlet and Outlet)

일반 설명

Device Configuration: Gamma Gold Capsule

포장

Blister

기타 정보

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

제조 메모

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).

분석 메모

Bacterial Retention
Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
Gravimetric Extractables: using sterilized device after a 200 mL flush and 24 hours in water at controlled room temperature
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥200 mL

법적 정보

ASTM is a registered trademark of American Society for Testing and Materials
Durapore is a registered trademark of Merck KGaA, Darmstadt, Germany
Emprove is a registered trademark of Merck KGaA, Darmstadt, Germany
MILLIPAK is a registered trademark of Merck KGaA, Darmstadt, Germany

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