| Primary Device ID | 00846832078509 |
| NIH Device Record Key | 9d27bb68-4e9a-4f04-b262-7091f9f56464 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PERFORM™ HUMERAL SYSTEM |
| Version Model Number | DWT3330 |
| Catalog Number | DWT3330 |
| Company DUNS | 968990812 |
| Company Name | TORNIER, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com |
| Outer Diameter | 33 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 33 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 33 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 33 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 33 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 33 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 33 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 33 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 33 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 33 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 33 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 33 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00846832078509 [Primary] |
| PAO | prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2022-03-29 |
| Device Publish Date | 2020-11-10 |