| Primary Device ID | 05060077232488 |
| NIH Device Record Key | 6e20dffa-abd4-42e5-bb3d-21bc5d834d93 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KerraFoam Gentle Border |
| Version Model Number | 6 x 6in |
| Catalog Number | CWL1132 |
| Company DUNS | 543740310 |
| Company Name | CRAWFORD HEALTHCARE LIMITED |
| 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 | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05060077232464 [Primary] |
| GS1 | 05060077232471 [Package] Contains: 05060077232464 Package: Carton [10 Units] In Commercial Distribution |
| GS1 | 05060077232488 [Package] Contains: 05060077232471 Package: Shipper [4 Units] In Commercial Distribution |
| 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 | 2019-10-09 |
| Device Publish Date | 2019-10-01 |
| 05060077232617 | 7 x 8in |
| 05060077232549 | 4 x 12in |
| 05060077232518 | 4 x 10in |
| 05060077232488 | 6 x 6in |
| 05060077231399 | 9 x 10in |
| 05060077232662 | 6.7 x 6.9in |
| 05060077232679 | 9.8 x 9in |
| 05060077232648 | 5 x 5in |
| 05060077232655 | 4 x 8in |
| 05060077232631 | 4 x 4in |
| 05060077230699 | 3 x 3in |