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Merck

KVEPS015HB3

Millipore

Millipore Express® SHR 0.1µm, Opticap® XL 150 Capsule

Fittings 9/16 in. HB/HB with Bell, Sterile

别名:

Millipore Express®SHR, Opticap® XL 囊式

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About This Item

分類程式碼代碼:
23151806
价格与库存信息目前不能提供

产品名称

Opticap 无菌 XL 150 Millipore Express SHR 单层 0.1 µm 9/16 in.HB/带灌注钟罩的 HB, Opticap® XL 150, sterile, inlet connection diam. 9/16 in., cartridge nominal length 3.8 in. (9.7 cm)

材料

polyethersulfone
polyethylene support
polypropylene
polypropylene housing
polypropylene vent cap
silicone seal

品質等級

法律遵循

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

無菌

irradiated
sterile

產品線

Opticap® XL 150

特點

hydrophilic

製造商/商標名

Millipore Express®

參數

≤1.4 mL/min air diffusion at 3.45 bar (50 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 23 °C (intermittent)
80 psi max. differential pressure (5.5 bar) (continuous)
80 psig max. inlet pressure

技術

sterile filtration: suitable

長度

9.7 cm (3.8 in.)

柱標稱長度

3.8 in. (9.7 cm)

直徑

5.6 cm (2.2 in.)

過濾面積

250 cm2

入口接頭直徑

9/16 in.

入口到出口寬度

9.7 cm (3.8 in.)

出口接頭直徑

9/16 in.

雜質

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

基質

Millipore Express® SHR

孔徑

0.1 μm

起泡點

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

接頭

1/4 in. drain/vent hose barb (with double O-ring Seal)
(14 mm (9/16 in.) Sanitary Flange Inlet and 14 mm (9/16 in.) Outlet with filling bell)

相关类别

一般說明

Device Configuration: 取样皿滤膜

包裝

Double Easy-Open bag

其他說明

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 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.

準備報告

Sterilization Method
3 autoclave cycles of 60 min @ 123 °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).

分析報告

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 2.0 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 ≥1 L

法律資訊

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

免責聲明

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.

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