Primary Device ID | 10351688835802 |
NIH Device Record Key | 3d00e921-3983-4095-aac3-c38bdeda7ab8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bivona |
Version Model Number | FU14LN60NSA087N |
Company DUNS | 118112924 |
Company Name | SMITHS MEDICAL ASD, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | 10351688835802 [Primary] |
JOH | Tube tracheostomy and tube cuff |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10351688835802]
Moist Heat or Steam Sterilization
[10351688835802]
Moist Heat or Steam Sterilization
[10351688835802]
Moist Heat or Steam Sterilization
[10351688835802]
Moist Heat or Steam Sterilization
[10351688835802]
Moist Heat or Steam Sterilization
[10351688835802]
Moist Heat or Steam Sterilization
[10351688835802]
Moist Heat or Steam Sterilization
[10351688835802]
Moist Heat or Steam Sterilization
[10351688835802]
Moist Heat or Steam Sterilization
[10351688835802]
Moist Heat or Steam Sterilization
[10351688835802]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2024-09-12 |
Device Publish Date | 2015-09-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BIVONA 85655728 4333915 Live/Registered |
Ippolito, Alessandro 2012-06-19 |
BIVONA 76406546 2726803 Live/Registered |
SMITHS MEDICAL ASD, INC. 2002-05-13 |
BIVONA 74023385 1655884 Dead/Cancelled |
Bivona Inc. 1990-01-29 |
BIVONA 73735715 1563202 Dead/Cancelled |
BIVONA INC. 1988-06-21 |