| Primary Device ID | 00889024581111 |
| NIH Device Record Key | d1a17f4e-5bf3-4af1-9b88-7c0cb69b6210 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DEPUY STYLE CAN GLEN REMR MSTR |
| Version Model Number | SSI005285 |
| Catalog Number | SSI005285 |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 | 00889024581111 [Primary] |
| KWT | PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-01-21 |
| Device Publish Date | 2020-01-13 |
| 00880304858992 - JUGGERKNOT | 2025-09-22 |
| 00880304404809 - MINI RC NEEDLE | 2025-09-08 |
| 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 |