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Opticap® XL2 Durapore®

品牌
Millipore
货号
KVGLA02FF3
规格纯度
sterile, inlet connection diam. 3/4 in., pore size 0.22 μm, cartridge nominal length 2 in. (5 cm)
参考价格
4481.58 *本价格含增值税费
促销
数量
-+
产品介绍:

产品说明

一般描述

Device Configuration: 取样皿滤膜

包装

Double Easy-Open bag

其他说明

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.

联系

Replaces: KVGL04FF3

制备说明

Sterilization Method
3 autoclave cycles of 60 min @ 126 °C; 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).

分析说明

Gravimetric Extractables: after 24 hours in water at controlled room temperature
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥500 mL
Bacterial Retention
Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.

法律信息

ASTM is a registered trademark of American Society for Testing and Materials
Durapore is a registered trademark of Merck KGaA, Darmstadt, Germany
Emprove is a registered trademark of Merck KGaA, Darmstadt, Germany
OPTICAP is a registered trademark of Merck KGaA, Darmstadt, Germany

免责声明

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.

产品性质

质量水平400
物料PVDF
polypropylene
polypropylene housing
polypropylene support
polypropylene vent cap
silicone seal
reg. compliancemeets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
无菌性sterile
产品线EMPROVE® Filter
特点hydrophilic
manufacturer/tradenameOpticap®
参数1.0 bar max. differential pressure (15 psid) at 80 ℃ (Forward)
1.0 bar max. inlet pressure (15 psi) at 80 ℃
2.8 bar max. inlet pressure (40 psi) at 60 ℃
25 ℃ max. inlet temp.
3.4 bar max. differential pressure (50 psid) at 25 ℃ (Reverse; intermittent)
5.5 bar max. differential pressure (80 psid) at 25 ℃ (Forward)
5.5 bar max. inlet pressure (80 psi) at 23 ℃
80 psig max. inlet pressure
长度13.5 cm (5.3 in.)
cartridge nominal length2 in. (5 cm)
直径12.5 cm (4.9 in.)
过滤面积0.09 m2
inlet connection diam.3/4 in.
inlet to outlet W13.5 cm (5.3 in.)
outlet connection diam.3/4 in.
总尺寸2 in.
杂质≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)
<0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
gravimetric extractables≤10 mg/capsule
基质Durapore®
孔径0.22 μm nominal pore size
0.22 μm pore size
inputsample type liquid
bubble point≥3450 mbar (50 psig), air with water at 23 ℃
配件1/4 in. drain/vent hose barb (with double O-ring Seal)
inlet sanitary flange
19 mm (3/4 in.) inlet/outlet sanitary flange
outlet sanitary flange

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