| Primary Device ID | 00714196390820 | 
| NIH Device Record Key | a0c8ccea-71f3-4e7b-9b6d-3cd74687b64e | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | ComfortFoam Border | 
| Version Model Number | 43412 | 
| 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 | 00714196390820 [Primary] | 
| NAD | Dressing, Wound, Occlusive | 
| 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 | 
| 00714196437709 | 43770 | 
| 00714196436801 | 43680 | 
| 00714196434807 | 43480 | 
| 00714196434128 | 43412 | 
| 00714196433305 | 43330 | 
| 00714196432506 | 43250 | 
| 00714196432209 | 43220 | 
| 00714196318664 | 00318E | 
| 00714196317445 | 00317E | 
| 00714196390882 | 43770 | 
| 00714196390868 | 43680 | 
| 00714196390844 | 43480 | 
| 00714196390820 | 43412 | 
| 00714196390806 | 43330 | 
| 00714196390783 | 43250 | 
| 00714196390769 | 43220 | 
| 00714196390745 | 00318E | 
| 00714196390721 | 00317E |