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Merck

KVGLG10FF1

Millipore

Cápsula Durapore® 0,22 µm. Opticap® XL

inlet connection diam. 3/4 in., Opticap® XL 10, cartridge nominal length 10 in. (25 cm)

Sinônimo(s):

Opticap Gamma Compatible XL10 Durapore 0.22 μm 3/4 in. TC/TC

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About This Item

Código UNSPSC:
23151806

Materiais

PVDF
polyester support
polyethylene support
polypropylene (gamma-stable)
polypropylene housing
polypropylene vent cap
silicone outer O-ring
silicone-coated EPDM rubber lead O-ring

Nível de qualidade

conformidade reg.

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

esterilidade

non-sterile

Compatibilidade de esterilização

gamma compatible

linha de produto

Opticap® XL 10

Características

gamma compatible
hydrophilic

fabricante/nome comercial

Opticap®

Parâmetros

≤14 mL/min air diffusion at 2.75 bar (40 psig) and 23 °C (in water)
1.0 bar max. inlet pressure (15 psi) at 80 °C
1.7 bar max. differential pressure (25 psid) at 80 °C (Forward)
2.8 bar max. inlet pressure (40 psi) at 60 °C
25 °C max. inlet temp.
3.5 bar max. differential pressure (50 psid) at 25 °C (Reverse; intermittent)
5.5 bar max. differential pressure (80 psid) at 25 °C (Forward)
5.5 bar max. inlet pressure (80 psi) at 23 °C
80 psig max. inlet pressure

técnica(s)

sterile filtration: suitable

Comprimento

13.2 in.

Largura

4.2 in.

comprimento nominal do cartucho

10 in. (25 cm)

Diâmetro

10.7 cm (4.2 in.)

área de filtração

0.73 m2

diâm. conexão de entrada

3/4 in.

diam. conexão de saída

3/4 in.

Impurezas

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

extraíveis gravimétricos

≤25 mg/capsule

matriz

Durapore®

tamanho de poro

0.22 μm

entrada

sample type liquid

ponto de bolha

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

conector

1/4 in. drain/vent hose barb (with double O-ring Seal)
(19 mm (3/4 in.) Sanitary Flange Inlet and 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 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.

Nota de preparo

Sterilization Method
3 autoclave cycles of 60 min @ 126 °C; capable of 45 kilogray (4.5 Megarad) gamma exposure; 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).

Nota de análise

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 ≥1 L

Informações legais

ASTM is a registered trademark of American Society for Testing and Materials
Durapore 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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