| Primary Device ID | 14063108102406 |
| NIH Device Record Key | 7e034686-3d52-4f38-b293-90af2550943d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TRACHEOBRONXANE™ DUMON® RADIOPAQUE |
| Version Model Number | 09031RS |
| Company DUNS | 777211640 |
| Company Name | NOVATECH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 14063108102406 [Primary] |
| NWA | Prosthesis, Tracheal, Preformed/Molded |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-12-02 |
| Device Publish Date | 2024-11-22 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TRACHEOBRONXANE 76499541 2829546 Dead/Cancelled |
Novatech SA 2003-03-21 |
![]() TRACHEOBRONXANE 75699748 not registered Dead/Abandoned |
NOVATECH SA 1999-05-07 |