| Primary Device ID | 03700434023183 |
| NIH Device Record Key | 81f637fc-3858-4865-86f0-d35859a2afd8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AEQUALIS REVERSED FRACTURE |
| Version Model Number | DWD861 |
| Catalog Number | DWD861 |
| 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 | true |
| 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 |
| Phone | +330476613500 |
| order@tornier.com | |
| Phone | +330476613500 |
| order@tornier.com | |
| Phone | +330476613500 |
| order@tornier.com | |
| Phone | +330476613500 |
| order@tornier.com | |
| Phone | +330476613500 |
| order@tornier.com | |
| Phone | +330476613500 |
| order@tornier.com | |
| Phone | +330476613500 |
| order@tornier.com | |
| Phone | +330476613500 |
| order@tornier.com | |
| Phone | +330476613500 |
| order@tornier.com | |
| Phone | +330476613500 |
| order@tornier.com | |
| Phone | +330476613500 |
| order@tornier.com | |
| Phone | +330476613500 |
| order@tornier.com | |
| Phone | +330476613500 |
| order@tornier.com | |
| Phone | +330476613500 |
| order@tornier.com | |
| Phone | +330476613500 |
| order@tornier.com | |
| Phone | +330476613500 |
| order@tornier.com | |
| Phone | +330476613500 |
| order@tornier.com |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 36 Millimeter |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03700434023183 [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 | 2024-07-04 |
| Device Publish Date | 2024-06-26 |