| Primary Device ID | 00850065007229 |
| NIH Device Record Key | 3c22d002-ac12-4601-b198-e88d2f1ae053 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SM ORGANIZER |
| Version Model Number | 1007760 |
| Catalog Number | 1007760 |
| Company DUNS | 045657305 |
| Company Name | HF ACQUISITION CO. 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 | true |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850065007229 [Primary] |
| 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 | 2020-08-25 |
| Device Publish Date | 2020-08-17 |
| 00850065007229 | 1007760 |
| 00850065007267 | SM ORGANIZER |