| Primary Device ID | 00846832084043 |
| NIH Device Record Key | 761b270d-fed6-4837-ac45-44ba49b12aa4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tornier Perform |
| Version Model Number | MWM100 |
| Catalog Number | MWM100 |
| Company DUNS | 968990812 |
| Company Name | TORNIER, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | true |
| Serial Number | false |
| 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 |
| Length | 100 Millimeter |
| Outer Diameter | 3 Millimeter |
| Length | 100 Millimeter |
| Outer Diameter | 3 Millimeter |
| Length | 100 Millimeter |
| Outer Diameter | 3 Millimeter |
| Length | 100 Millimeter |
| Outer Diameter | 3 Millimeter |
| Length | 100 Millimeter |
| Outer Diameter | 3 Millimeter |
| Length | 100 Millimeter |
| Outer Diameter | 3 Millimeter |
| Length | 100 Millimeter |
| Outer Diameter | 3 Millimeter |
| Length | 100 Millimeter |
| Outer Diameter | 3 Millimeter |
| Length | 100 Millimeter |
| Outer Diameter | 3 Millimeter |
| Length | 100 Millimeter |
| Outer Diameter | 3 Millimeter |
| Length | 100 Millimeter |
| Outer Diameter | 3 Millimeter |
| Length | 100 Millimeter |
| Outer Diameter | 3 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00846832084043 [Primary] |
| FZX | Guide, surgical, instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-08-17 |
| Device Publish Date | 2022-08-09 |
| 00846832091959 | Posterior Glenoid Retractor |
| 00846832084043 | Guide Pin |
| 00846832084036 | 10° Retentive Reversed Insert Trial |
| 00846832084029 | 10° Retentive Reversed Insert Trial |
| 00846832084012 | 10° Reversed Insert Trial |
| 00846832084005 | 10° Retentive Reversed Insert Trial |
| 00846832083992 | 10° Reversed Insert Trial |
| 00846832083985 | 10° Retentive Reversed Insert Trial |
| 00846832083978 | 10° Reversed Insert Trial |
| 00846832083961 | 10° Reversed Insert Trial |
| 00846832083954 | 10° Reversed Insert Trial |
| 00846832083947 | 10° Retentive Reversed Insert Trial |
| 00846832083930 | 10° Retentive Reversed Insert Trial |
| 00846832083923 | 10° Reversed Insert Trial |
| 00846832083916 | 10° Reversed Insert Trial |
| 00846832083909 | 10° Retentive Reversed Insert Trial |
| 00846832083893 | 10° Retentive Reversed Insert Trial |
| 00846832083886 | 10° Reversed Insert Trial |
| 00846832083879 | 10° Retentive Reversed Insert Trial |
| 00846832083862 | 10° Retentive Reversed Insert Trial |
| 00846832083855 | 10° Reversed Insert Trial |
| 00846832083848 | 10° Retentive Reversed Insert Trial |
| 00846832083831 | 10° Retentive Reversed Insert Trial |
| 00846832083824 | 10° Reversed Insert Trial |
| 00846832083817 | 10° Reversed Insert Trial |
| 00846832083800 | 10° Retentive Reversed Insert Trial |
| 00846832083794 | 10° Reversed Insert Trial |
| 00846832083787 | 10° Retentive Reversed Insert Trial |
| 00846832083770 | 10° Reversed Insert Trial |
| 00846832083763 | 10° Retentive Reversed Insert Trial |
| 00846832083756 | 10° Reversed Insert Trial |
| 00846832083749 | 10° Reversed Insert Trial |
| 00846832083732 | 10° Reversed Insert Trial |
| 00846832083725 | 10° Retentive Reversed Insert Trial |
| 00846832083718 | 10° Reversed Insert Trial |
| 00846832083701 | 10° Reversed Insert Trial |
| 00846832083695 | 10° Retentive Reversed Insert Trial |
| 00846832083688 | 10° Retentive Reversed Insert Trial |
| 00846832083671 | Reversed Insert Trial |
| 00846832083664 | Retentive Reversed Insert Trial |
| 00846832083657 | Reversed Insert Trial |
| 00846832083640 | Reversed Insert Trial |
| 00846832083633 | Reversed Insert Trial |
| 00846832083626 | Retentive Reversed Insert Trial |
| 00846832083619 | Reversed Insert Trial |
| 00846832083602 | Retentive Reversed Insert Trial |
| 00846832083596 | Reversed Insert Trial |
| 00846832083589 | Retentive Reversed Insert Trial |
| 00846832083572 | Reversed Insert Trial |
| 00846832083565 | Retentive Reversed Insert Trial |