Primary Device ID | 00707387793517 |
NIH Device Record Key | 86e9aabc-41fe-4cd3-94df-238577b2a1b1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tegaderm |
Version Model Number | Alginate |
Catalog Number | 90220 |
Company DUNS | 770434090 |
Company Name | ADVANCED MEDICAL SOLUTIONS LIMITED |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00707387793517 [Primary] |
NAC | Dressing, Wound, Hydrophilic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-15 |
Device Publish Date | 2022-12-07 |
00707387793531 | Alginate Dressing |
04054596862067 | 1-2B, High Integrity |
04054596862043 | 1-2B, High Integrity |
04054596860995 | Hydrogel |
00707387793517 | 1-21B, High Gelling |
00707387583620 | 14-24AP Silver Alginate II |
00707387583613 | 14-24AP Silver Alginate II |
00707387583606 | 14-24AP Silver Alginate II |
00707387583590 | 14-24AP Silver Alginate II |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TEGADERM 77480670 3557085 Live/Registered |
3M Company 2008-05-21 |
TEGADERM 73380382 1256605 Live/Registered |
Minnesota Mining and Manufacturing Company 1982-08-17 |