| Primary Device ID | 08404535022155 |
| NIH Device Record Key | 40d04b0a-f6e9-49bc-ae57-1b0ab360018a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BrioPrep Sterile Diamonds |
| Version Model Number | 5031881U0 |
| Catalog Number | 5031881U0 |
| Company DUNS | 082080136 |
| Company Name | Peter Brasseler Holdings, 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 | false |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08404535022155 [Primary] |
| DZP | INSTRUMENT, DIAMOND, DENTAL |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2026-03-06 |
| Device Publish Date | 2025-11-21 |
| 08404535022186 | BRIO6368.31.020 (C) FTBALL 25P |
| 08404535022155 | BRIO5856.31.023 (SC) RD TAP 25P |
| 08404535022124 | BRIO8368.31.020 (F) FTBALL 25P |
| 08404535022001 | BRIO6830.31.012 (C) PEAR 25P |
| 08404535021974 | BRIO6859.31.014 (C) NEEDLE 25P |
| 08404535021943 | BRIO859EF.31.014 (EF) NDLE 25P |
| 08404535021912 | BRIO6837.31.012 (C) FLT CYLN 25P |
| 08404535021882 | BRIO368EF.31.023 (EF) FTBLL 25P |
| 08404535021851 | BRIO830L.31.012 (M) PEAR 25P |
| 08404535021820 | BRIO8379.31.025 (F) FTBALL 25P |
| 08404535021790 | BRIO6909.31.040 (C) WHEEL 25P |
| 08404535021769 | BRIO8859.31.014 (F) NEEDLE 25P |