FDA UDI In Commercial Distribution 🇺🇸 United States

TiBrid-SA

DI: 00843511113049 · Model: 17-5A-AWL2 · OMNIA MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TiBrid-SA
Primary DI
00843511113049
Version / Model
17-5A-AWL2
Company Name
OMNIA MEDICAL, LLC
Labeler DUNS
079467378
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-12
Public Version
1
Public Version Date
2023-05-22
Public Version Status
New
Public Device Record Key
0ef58442-133a-462d-a0fb-385cb6a68672

Device Description

Awl, Punch

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

GMDN Terms

Code Name
15275 Bone awl, reusable

Identifiers

Type ID
Primary 00843511113049

Customer Contacts

Phone
3044134851

Premarket Submissions

Submission Number Supplement Number
K203207 000