Primary Device ID | 14063108101737 |
NIH Device Record Key | 1b714b4e-6fe7-436a-b45f-36617ca393e0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TRACHEOBRONXANE™ DUMON® RADIOPAQUE |
Version Model Number | 04291RS |
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 | 14063108101737 [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 | 2024-11-27 |
Device Publish Date | 2024-11-19 |
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 |