FDA UDI In Commercial Distribution 🇺🇸 United States

VANGUARD DA 360

DI: 00880304501058 · Model: 32-422623 · Biomet Uk Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VANGUARD DA 360
Primary DI
00880304501058
Version / Model
32-422623
Catalog Number
32-422623
Company Name
Biomet Uk Ltd
Labeler DUNS
219322575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-28
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
9f05b075-f603-4ff3-b9b4-48ccbaaf50c8

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
Yes
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
60411 Arthrodesis nail, non-sterile

Identifiers

Type ID
Primary 00880304501058

Customer Contacts