Primary Device ID | 00843511111809 |
NIH Device Record Key | baa8fb11-8868-4b76-8b7c-d02e864c8f61 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TiBrid™-SA |
Version Model Number | 17-0A-CVR0 |
Company DUNS | 079467378 |
Company Name | OMNIA MEDICAL, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | false |
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 | 3044134851 |
customerservice@omniamedical.com | |
Phone | 3044134851 |
customerservice@omniamedical.com | |
Phone | 3044134851 |
customerservice@omniamedical.com | |
Phone | 3044134851 |
customerservice@omniamedical.com | |
Phone | 3044134851 |
customerservice@omniamedical.com | |
Phone | 3044134851 |
customerservice@omniamedical.com | |
Phone | 3044134851 |
customerservice@omniamedical.com | |
Phone | 3044134851 |
customerservice@omniamedical.com | |
Phone | 3044134851 |
customerservice@omniamedical.com | |
Phone | 3044134851 |
customerservice@omniamedical.com | |
Phone | 3044134851 |
customerservice@omniamedical.com | |
Phone | 3044134851 |
customerservice@omniamedical.com | |
Phone | 3044134851 |
customerservice@omniamedical.com | |
Phone | 3044134851 |
customerservice@omniamedical.com | |
Phone | 3044134851 |
customerservice@omniamedical.com | |
Phone | 3044134851 |
customerservice@omniamedical.com | |
Phone | 3044134851 |
customerservice@omniamedical.com |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00843511111809 [Primary] |
OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00843511111809]
Moist Heat or Steam Sterilization
[00843511111809]
Moist Heat or Steam Sterilization
[00843511111809]
Moist Heat or Steam Sterilization
[00843511111809]
Moist Heat or Steam Sterilization
[00843511111809]
Moist Heat or Steam Sterilization
[00843511111809]
Moist Heat or Steam Sterilization
[00843511111809]
Moist Heat or Steam Sterilization
[00843511111809]
Moist Heat or Steam Sterilization
[00843511111809]
Moist Heat or Steam Sterilization
[00843511111809]
Moist Heat or Steam Sterilization
[00843511111809]
Moist Heat or Steam Sterilization
[00843511111809]
Moist Heat or Steam Sterilization
[00843511111809]
Moist Heat or Steam Sterilization
[00843511111809]
Moist Heat or Steam Sterilization
[00843511111809]
Moist Heat or Steam Sterilization
[00843511111809]
Moist Heat or Steam Sterilization
[00843511111809]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-03-27 |
Device Publish Date | 2024-03-19 |
00843511113131 | TiBrid™-SA SCREW COVER, 18mm |
00843511113124 | TiBrid™-SA SCREW COVER, 16mm |
00843511113117 | TiBrid™-SA SCREW COVER, 14mm |
00843511111816 | TiBrid™-SA SCREW COVER, 12mm |
00843511111809 | TiBrid™-SA SCREW COVER, 10mm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TIBRID 87649034 5846124 Live/Registered |
Omnia Medical 2017-10-17 |