Primary Device ID | 00846832077199 |
NIH Device Record Key | 40ec1fc2-5725-4d94-bbdb-d295a1902a7a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PERFORM™ HUMERAL SYSTEM |
Version Model Number | DWT5420 |
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 | |
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 |
Height | 20 Millimeter |
Outer Diameter | 54 Millimeter |
Height | 20 Millimeter |
Outer Diameter | 54 Millimeter |
Height | 20 Millimeter |
Outer Diameter | 54 Millimeter |
Height | 20 Millimeter |
Outer Diameter | 54 Millimeter |
Height | 20 Millimeter |
Outer Diameter | 54 Millimeter |
Height | 20 Millimeter |
Outer Diameter | 54 Millimeter |
Height | 20 Millimeter |
Outer Diameter | 54 Millimeter |
Height | 20 Millimeter |
Outer Diameter | 54 Millimeter |
Height | 20 Millimeter |
Outer Diameter | 54 Millimeter |
Height | 20 Millimeter |
Outer Diameter | 54 Millimeter |
Height | 20 Millimeter |
Outer Diameter | 54 Millimeter |
Height | 20 Millimeter |
Outer Diameter | 54 Millimeter |
Height | 20 Millimeter |
Outer Diameter | 54 Millimeter |
Height | 20 Millimeter |
Outer Diameter | 54 Millimeter |
Height | 20 Millimeter |
Outer Diameter | 54 Millimeter |
Height | 20 Millimeter |
Outer Diameter | 54 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00846832077199 [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 | 2 |
Public Version Date | 2025-03-06 |
Device Publish Date | 2020-11-10 |