| Primary Device ID | 00846832090419 |
| NIH Device Record Key | b863b551-2012-48da-9dc1-52fe8f1d6cc1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tornier Perform® Reversed Glenoid |
| Version Model Number | DWJ033 |
| Catalog Number | DWJ033 |
| Company DUNS | 968990812 |
| Company Name | TORNIER, INC. |
| 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 | true |
| 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 |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Outer Diameter | 39 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00846832090419 [Primary] |
| KWS | PROSTHESIS, SHOULDER, SEMI-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 | 2022-05-03 |
| Device Publish Date | 2022-04-25 |