| Primary Device ID | 00714196113641 |
| NIH Device Record Key | 78ac6525-54d3-4a41-bb33-74167d633db1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sterile Bordered Gauze |
| Version Model Number | 11364 |
| Company DUNS | 883925562 |
| Company Name | DERMARITE INDUSTRIES LLC |
| Device Count | 50 |
| 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 | 00714196113641 [Primary] |
| GS1 | 01714196113640 [Unit of Use] |
| 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 | 2020-09-09 |
| Device Publish Date | 2020-09-01 |
| 00714196263667 | 00263E |
| 00714196262448 | 00262E |
| 00714196261229 | 00261E |
| 00714196114808 | 11480 |
| 00714196114501 | 11450 |
| 00714196114143 | 11414 |
| 00714196114105 | 11410 |
| 00714196113641 | 11364 |
| 00714196112309 | 11230 |
| 00714196390448 | 00263E |
| 00714196390424 | 00262E |
| 00714196390400 | 00261E |
| 00714196390387 | 11480 |
| 00714196390363 | 11450 |
| 00714196390349 | 11414 |
| 00714196390325 | 11410 |
| 00714196390301 | 11364 |
| 00714196390288 | 11230 |