| Primary Device ID | 05036912001458 |
| NIH Device Record Key | ce7423f0-49cc-4376-a485-1994d18bdb94 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LIQUIFIX Precision Open |
| Version Model Number | 72014033 |
| Company DUNS | 236059171 |
| Company Name | ADVANCED MEDICAL SOLUTIONS (PLYMOUTH) LIMITED |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05036912001441 [Primary] |
| GS1 | 05036912001458 [Package] Contains: 05036912001441 Package: Unit Carton [1 Units] In Commercial Distribution |
| GS1 | 05036912001465 [Package] Package: Shipper [6 Units] In Commercial Distribution |
| PLJ | Tissue Adhesive Internal Use |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-07-03 |
| Device Publish Date | 2023-06-23 |
| 05036912001427 - LIQUIFIX FIX8 | 2023-07-03 |
| 05036912001458 - LIQUIFIX Precision Open | 2023-07-03 |
| 05036912001458 - LIQUIFIX Precision Open | 2023-07-03 |
| 05036912000406 - LiquiBand Butyl | 2023-06-20 |
| 05036912001694 - LiquiBand Exceed | 2023-06-20 |
| 05036912001724 - LiquiBand Exceed XS | 2023-06-20 |
| 05036912001755 - LiquiBand Octyl Mini | 2023-06-20 |
| 05036912001519 - LiquiBand Secure | 2023-05-29 |
| 05036912001540 - LiquiBand Secure | 2023-05-29 |