FDA UDI In Commercial Distribution 🇺🇸 United States

Virage™

DI: 00889024329072 · Model: 07.01776.001 · BIOMET SPINE LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Virage™
Primary DI
00889024329072
Version / Model
07.01776.001
Catalog Number
07.01776.001
Company Name
BIOMET SPINE LLC
Labeler DUNS
018577570
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-23
Public Version
5
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
d3318d7f-92b7-4c00-984d-d3da4a8cca32

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
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00889024329072

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Tower Rod Reducer