一般描述
Device Configuration: 取样皿滤膜
特点和优势
Format: Single Layer
包装
Double Easy-Open bag
其他说明
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
制备说明
Sterilization Method 3 autoclave cycles of 30 min @ 126 °C; not in-line steam sterilizable
分析说明
Gravimetric Extractables: after 24 hours in water at controlled room temperature
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.
| 物料 | polypropylene polypropylene housing polypropylene support polypropylene vent cap silicone seal |
| 质量水平 | 400 |
| reg. compliance | meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials) |
| manufacturer/tradename | Opticap® |
| 参数 | 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 |
| 长度 | 21.6 cm (8.5 in.) |
| cartridge nominal length | 5 in. (12.5 cm) |
| 直径 | 10.7 cm (4.2 in.) |
| 过滤面积 | 0.18 m2 |
| inlet connection diam. | 9/16 in. |
| inlet to outlet W | 21.6 cm (8.5 in.) |
| outlet connection diam. | 9/16 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 | ≤25 mg/capsule |
| 基质 | Polygard®-CN |
| 孔径 | 10.0 μm nominal pore size 10.0 μm pore size |
| input | sample type liquid |
| 配件 | inlet hose barb 14 mm (9/16 in.) inlet/outlet hose barb outlet hose barb |
