| Primary Device ID | 00385640029476 |
| NIH Device Record Key | 5ebe79ff-719a-4af2-a36a-f9c5940b07ba |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | OM-1000-BR |
| Company DUNS | 965484699 |
| Company Name | SUMMIT MEDICAL, INC. |
| 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 | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| 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 | 00385640029476 [Primary] |
| KCT | Sterilization Wrap Containers, Trays, Cassettes & Other Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-08-09 |
| Device Publish Date | 2017-08-24 |
| 00385640083881 - INSTRUSAFE | 2024-11-19 |
| 00385640083898 - INSTRUSAFE | 2024-11-19 |
| 00385640083874 - INSTRUSAFE | 2024-11-18 |
| 00385640083836 - INSTRUSAFE | 2024-11-15 |
| 00385640083843 - INSTRUSAFE | 2024-11-15 |
| 00385640083850 - INSTRUSAFE | 2024-11-15 |
| 00385640083867 - INSTRUSAFE | 2024-11-15 |
| 00385640083805 - INSTRUSAFE | 2024-11-14 |