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Opticap® XL5 Millipore Express® SHF

产品编号:4061127
规格:sterile, inlet connection diam. 1.5 in., pore size 0.2 μm, cartridge nominal length 5 in. (12.5 cm)
包装规格:1 EA
产品类别:进口试剂
品牌:Millipore
优惠价:立即咨询
产品价格
产品编号包装单位单价(元)国内现货国外库存询价单
40611271 EA3690
产品别名

Opticap® XL5 Millipore Express® SHF

Opticap XL 5 Millipore Express SHF Sterile 0.2 μm 1-1/2 in. TC/TC

产品性质
Quality Level【质量水平】
400
material【物料】
polyester support
polyethersulfone
polypropylene (gamma-stable)
polypropylene housing
polypropylene vent cap
polysulfone
silicone seal
reg. compliance
meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
sterility【无菌性】
sterile
product line【产品线】
EMPROVE® Filter
feature【特点】
hydrophilic
manufacturer/tradename
Millipore Express®
parameter【参数】
≤17.4 mL/min air diffusion at 2.8 bar (40 psig) and 23 ℃ (in water)
1.0 bar max. differential pressure (15 psid) at 80 ℃ (Forward)
1.0 bar max. inlet pressure (15 psi) at 80 ℃
100 psi max. differential pressure (6.9 bar) (intermittent)
2.1 bar max. differential pressure (30 psid) at 25 ℃ (Reverse; intermittent)
2.75 bar max. inlet pressure (40 psi) at 60 ℃
25 ℃ max. inlet temp.
5.5 bar max. differential pressure (80 psid) at 25 ℃ (Forward)
5.5 bar max. inlet pressure (80 psi) at 25 ℃
6.9 bar max. differential pressure (100 psid) at 25 ℃ (Forward; intermittent)
6.9 bar max. inlet pressure (100 psi) at 25 ℃ (intermittent)
80 psi max. differential pressure (5.5 bar) (continuous)
80 psig max. inlet pressure
L【长度】
21.6 cm (8.5 in.)
cartridge nominal length
5 in. (12.5 cm)
diam.【直径】
10.7 cm (4.2 in.)
filtration area【过滤面积】
0.31 m2
inlet connection diam.
1.5 in.
inlet to outlet W
21.6 cm (8.5 in.)
outlet connection diam.
1.5 in.
overall size【总尺寸】
5 in.
impurities【杂质】
≤0.25 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)
<0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
matrix【基质】
Millipore Express® SHF
pore size【孔径】
0.2 μm nominal pore size
0.2 μm pore size
bubble point
≥4000 mbar (58 psig), air with water at 23 ℃
fitting【配件】
1/4 in. drain/vent hose barb (with double O-ring seal)
inlet sanitary flange
38 mm (1 1/2 in.) inlet/outlet sanitary flange
outlet sanitary flange
packaging【包装】
Double Easy-Open bag
基本信息
General description【一般描述】
Device Configuration: 取样皿滤膜
Sterile capsules meet current USP and AAMI guidelines for sterility utilizing a validated sterilization cycle.
Other Notes【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 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.

Preparation Note【制备说明】
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).
Sterilization Method
3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable
Analysis Note【分析说明】
TOC/Conductivity
After sterilization and a controlled water flush of 6.0 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
Bacterial Retention
Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
Legal Information【法律信息】
ASTM is a registered trademark of American Society for Testing and Materials
Emprove is a registered trademark of Merck KGaA, Darmstadt, Germany
MILLIPORE EXPRESS is a registered trademark of Merck KGaA, Darmstadt, Germany
OPTICAP is a registered trademark of Merck KGaA, Darmstadt, Germany
产品说明
Disclaimer【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.
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