| Primary Device ID | 00714196261229 | 
| NIH Device Record Key | 642a2166-22ca-46cd-9aae-858428f620c0 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Sterile Bordered Gauze | 
| Version Model Number | 00261E | 
| 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 | 00714196261229 [Primary] | 
| GS1 | 01714196261228 [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 |