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Merck
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Key Documents

KPGEG05TT1

Millipore

Millipore Express® PHF, Opticap® XL Capsule

Opticap® XL 5, inlet connection diam. 1.5 in., cartridge nominal length 5 in. (12.5 cm)

동의어(들):

Opticap XL 5 Millipore Express PHF Gamma Compatible 0.2 μm 1-1/2 in. TC/TC

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About This Item

UNSPSC 코드:
23151806

material

polyester support
polyethersulfone
polypropylene (gamma-stable)
polypropylene housing
polypropylene vent cap
polysulfone
silicone seal

Quality Level

규정 준수

meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)

무균

irradiated
non-sterile

멸균 적합성

gamma compatible

제품 라인

Opticap® XL 5

특징

gamma compatible
hydrophilic

제조업체/상표

Millipore Express®

파라미터

≤17.4 mL/min air diffusion at 2.8 bar (40 psig) and 23 °C (in water)
1.0 bar max. inlet pressure (15 psi) at 80 °C
1000 bar max. differential pressure (15 psi) at 80 °C
2.75 bar max. inlet pressure (40 psi) at 60 °C
25 °C max. inlet temp.
5.5 bar max. inlet pressure (80 psi) at 25 °C
5500 mbar max. differential pressure (80 psi) at 25 °C
80 psig max. inlet pressure

기술

bioburden reduction: suitable

길이

21.6 cm (8.5 in.)

너비

4.2 in.

카트리지 공칭 길이

5 in. (12.5 cm)

직경

10.7 cm (4.2 in.)

여과 면적

0.31 m2

입구 연결 직경

1.5 in.

입구에서 출구 너비(W)

21.6 cm (8.5 in.)

출구 연결 직경

1.5 in.

불순물

≤0.25 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)
<0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)

기질

Millipore Express® PHF

공극 크기

0.2 μm

피팅

1/4 in. drain/vent hose barb (with double O-ring seal)
inlet sanitary flange
outlet sanitary flange
(38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)

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일반 설명

Device Configuration: Capsule

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 of Filters with MILLIPORE EXPRESS® Membrane user guide
  • Storage Statement: Please refer Filters with MILLIPORE EXPRESS® Membrane user guide
  • Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

제조 메모

Sterilization Method
3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable
This product was manufactured with a Millipore Express® 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 of membrane used in this filter were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
TOC/Conductivity
After sterilization and a controlled water flush of 6.0 L, samples exhibited less than 500 ppb TOC per USP <64> and less than 1.3 µS/cm per USP <64> at 25 °C.
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L

법적 정보

ASTM is a registered trademark of American Society for Testing and Materials
MILLIPORE EXPRESS is a registered trademark of Merck KGaA, Darmstadt, Germany
OPTICAP is a registered trademark of Merck KGaA, Darmstadt, Germany

면책조항

EMD Millipore Corporation certifies that this product complies with the European Pressure Equipment Directive, 97/23/EC of 29 May 1997. This product has been classified under Article 3 § 3 of the Pressure Vessel Directive. It has been designed and manufactured in accordance with sound engineering practice to ensure safe use. In compliance with Article 3 § 3 of this Pressure Vessel Directive, this product does not bear the CE mark.

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