| Primary Device ID | 30653405986991 |
| NIH Device Record Key | 580153a7-7199-48c2-8486-e44efd4af61b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ExoShape |
| Version Model Number | 2101-02-012 |
| Catalog Number | 2101-02-012 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 30653405986991 [Primary] |
| LXH | Orthopedic manual surgical instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-06-10 |
| Device Publish Date | 2022-06-02 |
| 20845854082161 | EXOSHAPE SOFT TISSUE FASTENER FEMORAL, 11MM x 21 MM |
| 30845854082168 | EXOSHAPE SOFT TISSUE FASTENER FEMORAL 11 MM |
| 30845854082151 | EXOSHAPE SOFT TISSUE FASTENER FEMORAL 10 MM |
| 30845854082144 | EXOSHAPE SOFT TISSUE FASTENER FEMORAL 9 MM |
| 30845854082137 | EXOSHAPE SOFT TISSUE FASTENER FEMORAL 8 MM |
| 20653405986888 | EXOSHAPE SOFT TISSUE FASTENER TIBIAL, 12 MM x 30 MM |
| 20653405986871 | EXOSHAPE SOFT TISSUE FASTENER TIBIAL, 11 MM x 30 MM |
| 20653405986864 | EXOSHAPE SOFT TISSUE FASTENER TIBIAL, 10 MM x 30 MM |
| 20653405986857 | EXOSHAPE SOFT TISSUE FASTENER TIBIAL, 9 MM x 30 MM |
| 20653405986840 | EXOSHAPE SOFT TISSUE FASTENER TIBIAL, 8 MM x 30 MM |
| 20653405986833 | EXOSHAPE SOFT TISSUE FASTENER TIBIAL, 7 MM x 30 MM |
| 30653405987141 | ExoShape Sheath Inserter 10 mm |
| 30653405987042 | ExoShape Removal Tool Femoral |
| 30653405987035 | ExoShape Instrument Caddy |
| 10653405987024 | ExoShape Gun Tibial |
| 30653405987011 | ExoShape Removal Tool Tibial |
| 30653405987004 | ExoShape Graft Bar |
| 30653405986991 | ExoShape Sheath Inserter 12 mm |
| 30653405986984 | ExoShape Sheath Inserter 11 mm |
| 10653405986973 | ExoShape Sheath Inserter 9 mm |
| 10653405986966 | ExoShape Sheath Inserter 8 mm |
| 10653405986959 | ExoShape Sheath Inserter 7 mm |
| 30653405986946 | ExoShape Trialator 11 mm |
| 30653405986939 | ExoShape Trialator 10 mm |
| 10653405986928 | ExoShape Trialator 9 mm |
| 30653405986915 | ExoShape Trialator 8 mm |
| 30653405986908 | ExoShape Trialator 7 mm |
| 10653405986898 | ExoShape Trialator 6 mm |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() EXOSHAPE 85125012 3982761 Live/Registered |
CONMED CORPORATION 2010-09-08 |