FDA UDI In Commercial Distribution 🇺🇸 United States

OMNIMAX

DI: 00841036274689 · Model: 01-5924 · BIOMET MICROFIXATION, INC
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OMNIMAX
Primary DI
00841036274689
Version / Model
01-5924
Catalog Number
01-5924
Company Name
BIOMET MICROFIXATION, INC
Labeler DUNS
046189866
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-07
Public Version
3
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
e56f72b4-70cf-4fcc-804b-a8aaac9b6a70

Device Characteristics

Single Use
Yes
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
MR Conditional
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
HTY PIN, FIXATION, SMOOTH
JEY PLATE, BONE
DZL SCREW, FIXATION, INTRAOSSEOUS

GMDN Terms

Code Name
35685 Orthopaedic bone wire

Identifiers

Type ID
Primary 00841036274689

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K202969 000
K831005 000