| Primary Device ID | 05034480310125 |
| NIH Device Record Key | 3baff37c-19fb-4056-b4db-1bab1c5f7b24 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pall PharmAssure® 25 mm Hydrophobic Vent Filter |
| Version Model Number | HP2002 |
| Catalog Number | HP2002 |
| Company DUNS | 485050483 |
| Company Name | Pall International Sàrl |
| Device Count | 50 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)645-6578 |
| QAMedical@pall.com |
| Pore Size | 0.2 Micrometer |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05034480310125 [Primary] |
| GS1 | 25034480310129 [Unit of Use] |
| FMF | Syringe, piston |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-06-26 |
| Device Publish Date | 2016-07-27 |
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