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millipore Durapore 滤芯过滤0.22um

产品时间:2021-12-30

简要描述:

CVGL73TP3 millipore Durapore 滤芯过滤0.22um,MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

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CVGL73TP3 millipore Durapore 滤芯过滤0.22um

概述


Description
Catalogue NumberCVGL73TP3
Trade Name
  • Durapore®

DescriptionDurapore® Cartridge Filter 30 in. 0.22 µm Code 7

CVGL73TP3 millipore Durapore 滤芯过滤0.22um

Product Information
Device ConfigurationCartridge
Maximum Differential Pressure, bar (psid)Forward: 5.5 bar (80 psid) @ 25 °C; 1.7 bar (25 psid) @ 80 °C; 0.35 bar (5 psid) @ 135 °C. Reverse: 3.5 bar (50 psid) @ 25 °C
Maximum Inlet Pressure, bar (psi)Forward - 5.5 bar (80 psi) @ 25 °C; 1.7 bar (25 psi) @ 80 °C; 0.35 bar (5 psi) @ 135 °C; Reverse - 3.5 bar (50 psi) @ 25 °C
Cartridge CodeCode 7 (2-226) O-rings w/locking-tabs
Good Manufacturing PracticesThese products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Quality LevelMQ400
Biological Information
Bacterial EndotoxinsAqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
MediaDurapore®
SterilityOther
Sterilization30 SIP cycles of 30 min @ 135 °C; 30 autoclave cycles of 60 min @ 126 °C
Bacterial RetentionSamples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
WettabilityHydrophilic
Physicochemical Information
Pore Size0.22 µm
Air Diffusion at 23 °C≤40 mL/min @ 2.75 bar (40 psig) in water
Bubble Point at 23 °C≥3450 mbar (50 psig) air with water
Flow Rate50 L/min @ 460 mbar ΔP
Indirect Food AdditiveAll component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. All component materials meet the requirements of the EU framework regulation [1935/2004/EC] regarding materials and articles intended to contact food.
Non-Fiber ReleasingThis 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).
TOC/ConductivityAfter sterilization and a controlled water flush of 16.5 L, samples exhibited less than 500 ppb TOC per USP<643>and less than 1.3 µS/cm per USP<645>.
USP Bacterial EndotoxinsA sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
Materials Information
Chemistry
  • Polyvinylidene Fluoride (PVDF)

Device Material
  • Polypropylene

Seal MaterialSilicone (SI)
Support MaterialPolypropylene
理化信息
毛孔大小0.22微米
23°C时空气扩散在水中2.75 bar(40 psig)时≤40 mL / min
沸点23°C≥3450 mbar(50 psig)空气与水
流量50 L / min @ 460 mbarΔP
间接食品添加剂所有成分材料均符合21 CFR 177-182中引用的FDA间接食品添加剂要求。所有成分材料均符合欧盟框架法规[1935/2004 / EC]中有关与食品接触的材料和物品的要求。
非光纤释放此产物用的Durapore制造®满足的标准,“非纤维释放"过滤器如21 CFR 210.3(b)中(6)所定义的膜。
TOC /电导率灭菌和控制水冲洗量为16.5 L后,每个USP<643>样品的TOC小于500 ppb,每个USP<645>的样品TOC小于1.3 µS / cm。
USP细菌内毒素根据the变形细胞溶解液(LAL)试验测定,样品水提取物的含量少于0.5 EU / mL。
外型尺寸
墨盒标称长度30英寸(75厘米)
直径6.9厘米(2.7英寸)
过滤面积2.07平方米
装置尺寸30英寸
材料信息
化学
  • 聚偏二氟乙烯(PVDF)

设备材质
  • 聚丙烯

密封材料矽胶(是)
支撑材料聚丙烯
包装信息
材料尺寸3
材料包双重易开袋
技术指标
可氧化物质用水冲洗≥3 L后,将满足USP可氧化物质测试要求

上海登宁科技有限公司是国内专业的实验过滤材料提供商,致力于将质量、可靠性和操作性突出的产品带给每一位客户。
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