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Merck

KHGEA2TBB1

Millipore

Millipore Express® SHC, cápsula Opticap® XLT

inlet connection diam. 1 in., Opticap® XLT 20, pore size 0.5/0.2 μm, cartridge nominal length 20 in. (50 cm)

Sinónimos:

Opticap Autoclavable XLT 20 Millipore Express SHC 0.5/0.2 μm 1 in. HB/HB

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About This Item

Código UNSPSC:
23151806

Materiales

polyethersulfone
polypropylene
polypropylene housing
polypropylene support
polypropylene vent cap
polysulfone
silicone seal

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

autoclavable compatible

Línea del producto

Opticap® XLT 20

Características

hydrophilic

fabricante / nombre comercial

Millipore Express®

Parámetros

≤56.3 mL/min air diffusion at 2.8 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
100 psi max. differential pressure (6.9 bar) (intermittent)
2.1 bar max. differential pressure (30 psid) at 25 °C (Reverse; intermittent)
2.75 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
6.9 bar max. differential pressure (100 psid) at 25 °C (Forward; intermittent)
6.9 bar max. inlet pressure (100 psi) at 25 °C (intermittent)
80 psi max. differential pressure (5.5 bar) (continuous)
80 psig max. inlet pressure

técnicas

sterile filtration: suitable

Longitud

62.5 cm (24.6 in.)

Anchura

7.8 in.

longitud nominal del cartucho

20 in. (50 cm)

Diámetro

10.7 cm (4.2 in.)

filtración área

0.98 m2

diám. conexión a entrada

1 in.

An entrada a salida

19.8 cm (7.8 in.)

diám. conexión a salida

1 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® SHC

pore size

0.5/0.2 μm pore size

punto de burbuja

≥4000 mbar (58 psig), air with water at 23 °C

Adaptador

1/4 in. drain/vent hose barb (with double O-ring seal)
inlet hose barb
outlet hose barb
(25 mm (1 in.) Hose Barb Inlet and Outlet)

Descripción general

Device Configuration: Capsule
T-line/Gauge Port: T-line

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 installation section of OPTICAP® XL Capsules and OPTICAP® XLT Capsules 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; 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 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 of 40 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 ≥4 L

Información legal

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

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.

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