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Merck
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문서

CCGL52TP1

Millipore

Charged Durapore® 0.22 µm, Cartridge

cartridge nominal length 20 in. (50 cm), Code 5 (2-222; O-rings and spear)

동의어(들):

Charged Durapore Cartridge 20 in. 0.22 μm Code 5

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About This Item

UNSPSC 코드:
23151806
eCl@ss:
32031690

material

PVDF
polypropylene
polypropylene support
silicone seal

Quality Level

무균

non-sterile

멸균 적합성

autoclavable compatible
steam-in-place compatible

제품 라인

Durapore®

특징

hydrophilic

제조업체/상표

Durapore®

파라미터

≤20 mL/min air diffusion at 2.1 bar (30 psig) and 23 °C (in water)
0.35 bar max. differential pressure (5 psid) at 135 °C (Forward)
0.35 bar max. inlet pressure (5 psi) at 135 °C (Forward)
1.7 bar max. differential pressure (25 psid) at 80 °C (Forward)
1.7 bar max. inlet pressure (25 psi) at 80 °C (Forward)
3.5 bar max. differential pressure (50 psid) at 25 °C (Reverse)
3.5 bar max. inlet pressure (50 psi) at 25 °C (Reverse)
45 L/min flow rate at 600 mbar (ΔP)
5.5 bar max. differential pressure (80 psid) at 25 °C (Forward)
5.5 bar max. inlet pressure (80 psi) at 25 °C (Forward)

기술

sterile filtration: suitable

길이

20 in.

카트리지 공칭 길이

20 in. (50 cm)

직경

6.9 cm (2.7 in.)

여과 면적

1.4 m2

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

≤40 mg/cartridge

기질

Charged Durapore®

공극 크기

0.22 μm

입력

sample type liquid

버블 포인트(bubble point)

≥2760 mbar (40 psig), air with water at 23 °C

카트리지 코드

Code 5 (2-222; O-rings and spear)

일반 설명

Device Configuration: Cartridge

포장

Double Easy-Open bag

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
10 SIP cycles of 30 min @ 135 °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).

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: after 24 hours in water at controlled room temperature
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥500 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

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