Primary Device ID | 00714196247032 |
NIH Device Record Key | de94dc54-1b23-4ab4-8f51-9cf2ceb02181 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DermaSyn |
Version Model Number | 00247 |
Company DUNS | 883925562 |
Company Name | DERMARITE INDUSTRIES LLC |
Device Count | 24 |
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 | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00714196247032 [Primary] |
GS1 | 10714196247039 [Unit of Use] |
NAE | Dressing, Wound, Hydrogel Without Drug And/Or Biologic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-09 |
Device Publish Date | 2020-09-01 |
00714196248084 | 00248 |
00714196247032 | 00247 |
00714196112460 | 11246 |
00714196112453 | 11245 |
71419624712486 | 00247 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DERMASYN 86187542 4601083 Live/Registered |
DermaRite Industries, LLC 2014-02-07 |
DERMASYN 78959427 not registered Dead/Abandoned |
Isolagen Technologies, Inc 2006-08-24 |