FDA UDI In Commercial Distribution 🇺🇸 United States

Virage®

DI: 00889024328112 · Model: 07.01707.032 · ZIMMER BIOMET INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Virage®
Primary DI
00889024328112
Version / Model
07.01707.032
Catalog Number
07.01707.032
Company Name
ZIMMER BIOMET INC
Labeler DUNS
045576443
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
6
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
53121c29-4fae-4be3-9739-a1f3fdb8bc0a

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
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
Yes
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
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00889024328112

Customer Contacts