| Primary Device ID | 03700386915451 |
| NIH Device Record Key | 78239ae3-22ce-4705-9e6c-ea69d3cea363 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AEQUALIS GLENOID |
| Version Model Number | DWB215 |
| Company DUNS | 260324876 |
| Company Name | TORNIER |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +330476613500 |
| order@tornier.com |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03700386915451 [Primary] |
| KWS | PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-12-23 |
| Device Publish Date | 2015-10-16 |
| 03700386915482 | DWB218 |
| 03700386915475 | DWB217 |
| 03700386915468 | DWB216 |
| 03700386915451 | DWB215 |
| 03700386915444 | DWB213 |
| 03700386915437 | DWB212 |
| 03700386915420 | DWB211 |
| 03700386915413 | DWB210 |
| 03700386915123 | DWB008 |
| 03700386915116 | DWB007 |
| 03700386915109 | DWB006 |
| 03700386915093 | DWB005 |
| 03700386915086 | DWB003 |
| 03700386915079 | DWB002 |
| 03700386915062 | DWB001 |