FDA UDI In Commercial Distribution 🇺🇸 United States

MG II®

DI: 00889024435995 · Model: 5110-43-23 · Zimmer, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MG II®
Primary DI
00889024435995
Version / Model
5110-43-23
Catalog Number
00-5110-043-23
Company Name
Zimmer, Inc.
Labeler DUNS
056038268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-25
Public Version
1
Public Version Date
2021-10-04
Public Version Status
New
Public Device Record Key
31a85203-7205-4c65-b3ae-4e894f8e3844

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
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
46585 Tibial insert

Identifiers

Type ID
Primary 00889024435995

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K892800 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Size E,F/Green, 23 mm