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Key Documents

5A10HH1

Millipore

Opticap® XL10 Polygard® CR

inlet connection diam. 9/16 in., pore size 25.0 μm, cartridge nominal length 10 in. (25 cm)

Sinónimos:

Opticap® XL10 Polygard®-CR 25 µm 9/16 in. HB/HB

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About This Item

UNSPSC Code:
23151806
eCl@ss:
32031690

material

polypropylene
polypropylene housing
polypropylene support
polypropylene vent cap
silicone seal

Quality Level

reg. compliance

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

manufacturer/tradename

Opticap®

parameter

1.0 bar max. inlet pressure (15 psi) at 80 °C
2.75 bar max. inlet pressure (40 psi) at 60 °C
25 °C max. inlet temp.
4.8 bar max. differential pressure (70 psid) at 20 °C
5.5 bar max. inlet pressure (80 psi) at 25 °C
80 psig max. inlet pressure

L

33.5 cm (13.2 in.)

cartridge nominal length

10 in. (25 cm)

diam.

10.7 cm (4.2 in.)

inlet connection diam.

9/16 in.

inlet to outlet W

33.5 cm (13.2 in.)

outlet connection diam.

9/16 in.

impurities

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

gravimetric extractables

≤55 mg/capsule

matrix

Polygard®-CR

pore size

25.0 μm nominal pore size
25.0 μm pore size

input

sample type liquid

fitting

inlet hose barb
14 mm (9/16 in.) inlet/outlet hose barb
outlet hose barb

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General description

Device Configuration: Capsule

Features and Benefits

Format: Single Layer

Packaging

Double Easy-Open bag

Other Notes

These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

Linkage

Replaces: KR2501HB1

Preparation Note

Sterilization Method
3 autoclave cycles of 30 min @ 126 °C; not in-line steam sterilizable

Analysis Note

Gravimetric Extractables: after 24 hours in water at controlled room temperature
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥5 L

Legal Information

OPTICAP is a registered trademark of Merck KGaA, Darmstadt, Germany
POLYGARD is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

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.

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»

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