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KPGEG015FH3

Millipore

Cápsula Millipore Express® PHF, Opticap® XL

Opticap® XL 150, inlet connection diam. 3/4 in., cartridge nominal length 3.8 in. (9.7 cm)

Sinônimo(s):

Opticap XL 150 Millipore Express PHF Gamma Compatible 0.2 μm 3/4 in. TC-9/16 in. HB

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About This Item

Código UNSPSC:
23151806

Materiais

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

Nível de qualidade

conformidade reg.

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

esterilidade

irradiated
non-sterile

Compatibilidade de esterilização

gamma compatible

linha de produto

Opticap® XL 150

Características

gamma compatible
hydrophilic

fabricante/nome comercial

Millipore Express®

Parâmetros

≤1.4 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

técnica(s)

bioburden reduction: suitable

Comprimento

9.7 cm (3.8 in.)

Largura

2.2 in.

comprimento nominal do cartucho

3.8 in. (9.7 cm)

Diâmetro

5.6 cm (2.2 in.)

área de filtração

220 cm2

diâm. conexão de entrada

3/4 in.

L entrada para a saída

9.7 cm (3.8 in.)

diam. conexão de saída

9/16 in.

Impurezas

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

matriz

Millipore Express® PHF

tamanho de poro

0.2 μm

conector

1/4 in. drain/vent hose barb (with double O-ring seal)
inlet sanitary flange
outlet hose barb
(19 mm (3/4 in.) Sanitary Flange Inlet and 14 mm (9/16 in.) Hose Barb Outlet)

Descrição geral

Device Configuration: Capsule

Embalagem

Double Easy-Open bag

Outras notas

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.

Nota de preparo

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).

Nota de análise

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 2.0 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

Informações legais

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

Exoneração de responsabilidade

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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