| Primary Device ID | 00860009716179 |
| NIH Device Record Key | 41fc81e0-5a08-42d0-b421-ec93b9ab6559 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ELASTIC BANDAGE |
| Version Model Number | 0314, 0393 |
| Company DUNS | 867236309 |
| Company Name | Jhk, Inc. |
| 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 | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | true |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860009716100 [Primary] |
| GS1 | 00860009716179 [Unit of Use] |
| FQM | BANDAGE, ELASTIC |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-08-07 |
| Device Publish Date | 2023-07-28 |
| 00860009716179 - ELASTIC BANDAGE | 2023-08-07 |
| 00860009716179 - ELASTIC BANDAGE | 2023-08-07 |
| 00860009716117 - EXTRACTOR, SPLINTER REMOVER | 2023-08-07 |
| 00860009716155 - SPRAY / PUMP | 2023-08-07 |
| 00860009716131 - SCALPEL, ONE-PIECE | 2023-08-07 |
| 00860009716148 - GAUZE / SPONGE, NONRESORBABLE FOR EXTERNAL USE | 2023-08-07 |
| 00860009716162 - PACK, HOT OR COLD, DISPOSABLE | 2023-08-07 |
| 00860009716193 - TAPE AND BANDAGE, ADHESIVE | 2023-08-07 |