KHGLS10FH1 MilliporeSterile Multilayer Durapore® Opticap® XL 10 in. 0.45 / 0.22 µm
Recommended Products
Overview
| Replacement Information |
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| Description | |
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| Catalogue Number | KHGLS10FH1 |
| Trade Name |
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| Description | Sterile Multilayer Durapore® Opticap® XL 10 in. 0.45 / 0.22 µm |
| References |
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| Product Information | |
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| Device Configuration | Capsule |
| Connections, Inlet/Outlet | Sanitary Flange/Hose Barb |
| European Pressure Equipment Directive | 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. |
| Good Manufacturing Practices | These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. |
| Quality Level | MQ400 |
| Applications |
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| Dimensions | |
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| Cartridge Nominal Length | 10 in. (25 cm) |
| Device Size | 10 in. |
| Inlet Connection Diameter | 3/4 in. |
| Outlet Connection Diameter | 9/16 in. |
| Materials Information | |
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| Chemistry |
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| Toxicological Information |
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| Safety Information according to GHS |
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| Safety Information |
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| Product Usage Statements |
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| Storage and Shipping Information |
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| Packaging Information | |
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| Material Size | 1 |
| Transport Information |
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| Supplemental Information |
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| Specifications |
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| Global Trade Item Number | |
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| Catalogue Number | GTIN |
| KHGLS10FH1 | 04053252379482 |
Documentation
Emprove Dossier
| Title | Version |
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| 2.0 |
Operational Excellence Dossier
| Title |
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Certificates of Quality
| Title |
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| Opticap XL 10 Capsule Multilayer Durapore Membrane C7JA39840 |
| Opticap XL 10 Capsule Multilayer Durapore Membrane C3KB37103 |
User Guides
| Title |
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| Opticap® XL Capsules and Opticap® XLT Capsules |