FDA UDI In Commercial Distribution 🇺🇸 United States

Vanguard®

DI: 00887868565991 · Model: 599305 · Biomet Orthopedics, LLC
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vanguard®
Primary DI
00887868565991
Version / Model
599305
Catalog Number
599305
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-13
Public Version
1
Public Version Date
2023-06-21
Public Version Status
New
Public Device Record Key
93cae8a7-7cb9-4451-9389-0a8e80c7e4e5

Device Characteristics

Single Use
No
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
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
MBH PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER
OIY Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 00887868565991

Customer Contacts