| Primary Device ID | 00860009615588 |
| NIH Device Record Key | 798bb5a9-e7cd-41fa-8c79-43376f49b445 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | US NAVY Reserve AED Kit |
| Version Model Number | 800-00076 |
| Company DUNS | 117667182 |
| Company Name | Nar Medical Depot, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | 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 | 00860009615588 [Primary] |
| OHO | First Aid Kit Without 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 | 2025-09-30 |
| Device Publish Date | 2025-09-22 |
| 00860009615588 - US NAVY Reserve AED Kit | 2025-09-30 |
| 00860009615588 - US NAVY Reserve AED Kit | 2025-09-30 |
| 00860009615595 - US NAVY Reserve AED Kit Refill | 2025-09-30 |
| 00860009615571 - TECC Training Kit | 2025-09-23 KIT, TECC TRAINING - FEMA, RESTOCK |
| 00860009615564 - Endotracheal Kit | 2025-07-29 KIT, ENDOTRACHEAL |
| 00860009615533 - Intubation Guide Kit | 2025-07-23 AIR Q KIT - SZ 3 |
| 00860009615540 - Intubation Guide Kit | 2025-07-23 AIR Q KIT - SZ 5 |
| 00860009615557 - Intubation Guide Kit | 2025-07-23 AIR Q KIT - SZ 4 |
| 00860009615526 - First Aid Kit | 2025-07-04 Micro Trauma First Aid Kit |