FDA UDI In Commercial Distribution 🇺🇸 United States

VANGUARD 360

DI: 00880304500006 · Model: 32-488474 · Biomet Orthopedics, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VANGUARD 360
Primary DI
00880304500006
Version / Model
32-488474
Catalog Number
32-488474
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
e37b400b-71fa-4d39-be56-ca3bf6560de2

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
MBV Prosthesis, knee, patello/femorotibial, semi-constrained, uhmwpe, pegged, cemented, polymer/metal/polymer
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
35297 Medullary canal orthopaedic reamer, flexible

Identifiers

Type ID
Primary 00880304500006

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K093293 000