FDA UDI In Commercial Distribution 🇺🇸 United States

Vanguard® Knee System

DI: 00880304272019 · Model: 183660 · Biomet Orthopedics, LLC
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vanguard® Knee System
Primary DI
00880304272019
Version / Model
183660
Catalog Number
183660
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
7
Public Version Date
2023-09-08
Public Version Status
Update
Public Device Record Key
1fb79536-f678-4156-a872-9a7207da7d91

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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
MBH PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER
HRY PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER
MBV Prosthesis, knee, patello/femorotibial, semi-constrained, uhmwpe, pegged, cemented, polymer/metal/polymer
OIY Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive

GMDN Terms

Code Name
46585 Tibial insert

Identifiers

Type ID
Primary 00880304272019

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 10 MM 79/83 MM