Primary Device ID | 14063108101379 |
NIH Device Record Key | 4a16981d-ed78-459b-8ad2-0e4e44bcd858 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TRACHEOBRONXANE™ DUMON® RADIOPAQUE |
Version Model Number | 03021RS |
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 | 14063108101379 [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 | 2024-11-21 |
Device Publish Date | 2024-11-13 |
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 |