| Primary Device ID | 00887868055409 |
| NIH Device Record Key | b0be8257-33df-4fbc-8ed6-cb66cfbbbcf3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | A.L.P.S.PROXIMAL RADIUS PLATE, SMALL |
| Version Model Number | 8513-18-400 |
| Catalog Number | 851318400 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, 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 | 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 | 00887868055409 [Primary] |
| HWC | Screw, fixation, bone |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-10-24 |
| 00887868571718 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571725 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571732 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571749 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571756 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571763 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571770 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571787 - RingLoc®+ Triflange | 2025-06-20 |