Saltar al contenido
Merck
Todas las fotos(1)

Key Documents

KVGLG04TT3

Millipore

Durapore® 0,22 µm, Opticap® XL Cápsula

Opticap® XL 4, inlet connection diam. 1.5 in., cartridge nominal length 4 in. (10 cm)

Sinónimos:

Opticap Gamma Compatible XL4 Durapore 0.22 μm 1-1/2 in. TC/TC

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización


About This Item

Código UNSPSC:
23151806

Materiales

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

Nivel de calidad

cumplimiento norm.

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

esterilidad

non-sterile

Compatibilidad de esterilización

gamma compatible

Línea del producto

Opticap® XL 4

Características

gamma compatible
hydrophilic

fabricante / nombre comercial

Opticap®

Parámetros

≤4.6 mL/min air diffusion at 2.75 bar (40 psig) and 23 °C (in water)
1.0 bar max. differential pressure (15 psid) at 80 °C (Forward)
1.0 bar max. inlet pressure (15 psi) at 80 °C
2.8 bar max. differential pressure (40 psid) at 25 °C (Reverse; intermittent)
2.8 bar max. inlet pressure (40 psi) at 60 °C
25 °C max. inlet temp.
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

técnicas

sterile filtration: suitable

Longitud

7.7 in.

Anchura

3.3 in.

longitud nominal del cartucho

4 in. (10 cm)

Diámetro

6.1 cm (2.4 in.)

filtración área

0.18 m2

diám. conexión a entrada

1.5 in.

diám. conexión a salida

1.5 in.

impurezas

≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)
<0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)

matriz

Durapore®

tamaño de poro

0.22 μm

entrada

sample type liquid

punto de burbuja

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

Adaptador

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

Descripción general

Device Configuration: Capsule

Envase

Double Easy-Open bag

Otras 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 preparación

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 análisis

Bacterial Retention
Samples 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, samples exhibited less than 500 ppb TOC per USP <64> and less than 1.3 µS/cm per USP <64> at 25 ºC.
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥500 mL

Información legal

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

Cláusula de descargo de responsabilidad

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.

¿No encuentra el producto adecuado?  

Pruebe nuestro Herramienta de selección de productos.


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico