| Primary Device ID | 10816058012325 |
| NIH Device Record Key | c1f78ba2-e680-4b00-861f-b1f6eb9ca679 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Kia |
| Version Model Number | 00083 ADU22 |
| Catalog Number | 00083 ADU22 |
| Company DUNS | 196527949 |
| Company Name | DC Safety Sales |
| 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 | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00816058012328 [Primary] |
| GS1 | 10816058012325 [Package] Contains: 00816058012328 Package: Bag [1 Units] In Commercial Distribution |
| GS1 | 30816058012329 [Package] Package: case (bagged) [12 Units] In Commercial Distribution |
| LRR | First Aid Kit With Drug |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-07-24 |
| Device Publish Date | 2023-07-14 |
| 10816058012318 | First Aid Kit Small |
| 10816058012127 | Severe Weather Kit |
| 10816058012325 | First Aid Kit |
| 10816058012172 | RAK Kit |