| Primary Device ID | 00714196392060 |
| NIH Device Record Key | 004174e1-cf4d-421c-b404-effe9ba60867 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DermaGinate |
| Version Model Number | 00275E |
| Company DUNS | 883925562 |
| Company Name | DERMARITE INDUSTRIES LLC |
| 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 | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00714196392060 [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 | 2021-09-17 |
| Device Publish Date | 2021-09-09 |
| 00714196275127 | 00275E |
| 00714196274120 | 00274E |
| 00714196272485 | 00272E |
| 00714196270443 | 00270E |
| 00714196260222 | 00260E |
| 00714196392060 | 00275E |
| 00714196392046 | 00274E |
| 00714196392008 | 00272E |
| 00714196391988 | 00270E |
| 00714196391964 | 00260E |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() DERMAGINATE 86028921 4470975 Live/Registered |
DermaRite Industries, LLC 2013-08-05 |