FDA UDI In Commercial Distribution 🇺🇸 United States

2.0MM SYSTEM

DI: 00841036219574 · Model: 91-2005-50 · BIOMET MICROFIXATION, INC
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
2.0MM SYSTEM
Primary DI
00841036219574
Version / Model
91-2005-50
Catalog Number
91-2005-50
Company Name
BIOMET MICROFIXATION, INC
Labeler DUNS
046189866
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-26
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
be86eb00-ed6e-4dbe-9ef6-94ac38afcd7f

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
HBW FASTENER, PLATE, CRANIOPLASTY
JEY PLATE, BONE
GWO Plate, cranioplasty, preformed, alterable
GXR COVER, BURR HOLE

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 00841036219574

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K121589 000
K121624 000