FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00841036272425 · Model: 323.1202 · BIOMET MICROFIXATION, INC
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00841036272425
Version / Model
323.1202
Catalog Number
323.1202
Company Name
BIOMET MICROFIXATION, INC
Labeler DUNS
046189866
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-23
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
7b5900a6-b6f4-4a26-9b33-4ba34bcba609

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
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
HWC Screw, fixation, bone
HRS Plate, fixation, bone

GMDN Terms

Code Name
61689 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 00841036272425
Previous 00854865007380

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K141241 000
K183317 000