Primary Device ID | 05036912000970 |
NIH Device Record Key | 9fef2059-5aca-4ef0-b7a6-c481f9d43752 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LiquiBand Flow Control |
Version Model Number | LFC002 |
Company DUNS | 236059171 |
Company Name | ADVANCED MEDICAL SOLUTIONS (PLYMOUTH) LIMITED |
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 | 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 | 05036912000413 [Package] Contains: 05036912000741 Package: Carton [12 Units] In Commercial Distribution |
GS1 | 05036912000741 [Primary] |
GS1 | 05036912000970 [Package] Contains: 05036912000413 Package: Shipper Carton [6 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 |
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 |
05036912001519 - LiquiBand Secure | 2023-05-29 |
05036912001540 - LiquiBand Secure | 2023-05-29 |