| Primary Device ID | B504OMTN190089900 |
| NIH Device Record Key | 5df0e4bc-0eca-4a14-9219-77d10fdee6e9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Conmed/Linvatec |
| Version Model Number | TN190-089-90 |
| Company DUNS | 016889401 |
| Company Name | Provision |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B504OMTN190089900 [Primary] |
| GFA | Blade, Saw, General & Plastic Surgery, Surgical |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-10-01 |
| Device Publish Date | 2018-08-29 |