FDA UDI In Commercial Distribution 🇺🇸 United States

MIMIX

DI: 00841036020965 · Model: 02-2005 · BIOMET MICROFIXATION, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MIMIX
Primary DI
00841036020965
Version / Model
02-2005
Company Name
BIOMET MICROFIXATION, INC
Labeler DUNS
046189866
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-11
Public Version
4
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
dd7785c1-fca6-41a1-b136-10f3324874ae

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GXP Methyl Methacrylate For Cranioplasty

GMDN Terms

Code Name
35217 Orthopaedic cement, non-antimicrobial

Identifiers

Type ID
Primary 00841036020965

Customer Contacts

Phone
904-741-4400

Premarket Submissions

Submission Number Supplement Number
K990290 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 5 grams