| Primary Device ID | 00887919258568 |
| NIH Device Record Key | 125da262-8d81-4ea7-bf74-57bb5d62a963 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Large Bone Blade |
| Version Model Number | 33820702 |
| Catalog Number | 33820702 |
| 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 | 00887919258568 [Primary] |
| GFA | BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-12-04 |
| Device Publish Date | 2025-11-26 |
| 08404535020892 - Forza+ | 2026-01-19 Forza+ Z5 1:5 FG |
| 08404535020922 - Forza+ | 2026-01-19 Forza+ Z1 1:1 Latch |
| 08404535020953 - Forza+ | 2026-01-19 Forza+ Z450 1:4.2 FG |
| 08404535020984 - Forza+ | 2026-01-19 Forza+ Z20 1:1 FG |
| 08404535021684 - Forza | 2026-01-19 Forza ELXT E Complete Set |
| 08404535021714 - Forza | 2026-01-19 Forza ELXT E-U Control Unit |
| 08404535021738 - Forza | 2026-01-19 FORZA EZ ENDO |
| 08404535021363 - Brasseler USA | 2025-12-25 DCP1F.RA DIACOMP + (F) POINT 5P |