Primary Device ID | 05036912001243 |
NIH Device Record Key | f16f4d1a-14a3-4095-9749-f89415c545df |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LiquiBand XL |
Version Model Number | 72014019 |
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 | |
Phone | +448444125754 |
Info@LiquiBand.com | |
Phone | +448444125754 |
Info@LiquiBand.com | |
Phone | +448444125754 |
Info@LiquiBand.com | |
Phone | +448444125754 |
Info@LiquiBand.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05036912001236 [Package] Package: Shipper Carton [6 Units] In Commercial Distribution |
GS1 | 05036912001243 [Package] Contains: 05036912001250 Package: Carton [2 Units] In Commercial Distribution |
GS1 | 05036912001250 [Primary] |
OMD | Cutaneous Tissue Adhesive With Mesh |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-06-08 |
Device Publish Date | 2022-05-31 |
05036912001489 | 72014046 |
05036912001397 | 72014027 |
05036912001243 | 72014019 |
05036912001663 | 72014046A |