| Primary Device ID | 05036912000871 |
| NIH Device Record Key | 5303a59e-fbb0-430f-b2c4-3d500f67a431 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LiquiBand Standard |
| Version Model Number | LB0002 |
| Company DUNS | 236059171 |
| Company Name | ADVANCED MEDICAL SOLUTIONS (PLYMOUTH) LIMITED |
| Device Count | 10 |
| 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 | 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 |
| Phone | +448444125754 |
| Info@LiquiBand.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05036912000321 [Primary] |
| GS1 | 05036912000642 [Unit of Use] |
| GS1 | 05036912000871 [Package] Contains: 05036912000321 Package: Shipper Carton [10 Units] In Commercial Distribution |
| MPN | Tissue Adhesive For The Topical Approximation Of Skin |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-06 |
| 05036912001595 - INTEGUSEAL | 2024-12-04 IS100 |
| 05036912001625 - INTEGUSEAL | 2024-12-04 IS200 |
| 05036912001427 - LIQUIFIX FIX8 | 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 |