FDA UDI In Commercial Distribution 🇺🇸 United States

MAXIM KNEE SYSTEM

DI: 00880304007284 · Model: 140072 · Biomet Orthopedics, LLC
Product Codes
10
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MAXIM KNEE SYSTEM
Primary DI
00880304007284
Version / Model
140072
Catalog Number
140072
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
4
Public Version Date
2022-10-24
Public Version Status
Update
Public Device Record Key
801cb0c1-924a-4688-9ae5-c0d64881b787

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
KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
LXT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE
HWC Screw, fixation, bone
HRS PLATE, FIXATION, BONE
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
HTY PIN, FIXATION, SMOOTH
MBH PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER
HTN WASHER, BOLT NUT
JDW PIN, FIXATION, THREADED
HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

GMDN Terms

Code Name
33745 Coated knee femur prosthesis

Identifiers

Type ID
Primary 00880304007284

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 65MM