| Primary Device ID | 00612649102313 |
| NIH Device Record Key | 90ad2a1f-346c-4ec0-9b98-caadca466de8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VIROBAC II®VIRAL/BACTERIAL FILTER |
| Version Model Number | 20801-50 |
| Catalog Number | 20801-50 |
| Company DUNS | 009299017 |
| Company Name | King Systems Corporation |
| Device Count | 1 |
| DM Exempt | false |
| 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 | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00612649102313 [Package] Contains: 00612649185590 Package: [50 Units] In Commercial Distribution |
| GS1 | 00612649185590 [Primary] |
| CAH | Filter, bacterial, breathing-circuit |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-21 |
| 00612649102337 | VII VIRAL/BACTERIAL FILTER |
| 00612649102313 | VII VIRAL/BACTERIAL FILTER |
| 00612649102290 | VII VIRAL/BACTERIAL FILTER |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VIROBAC II 75358800 2198262 Live/Registered |
King Systems Corporation 1997-09-18 |