FDA UDI In Commercial Distribution 🇺🇸 United States

Optio-C®

DI: 00889024329201 · Model: 07.01855.009 · ZIMMER SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Optio-C®
Primary DI
00889024329201
Version / Model
07.01855.009
Catalog Number
07.01855.009
Company Name
ZIMMER SPINE, INC.
Labeler DUNS
787663400
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
4
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
1ea14392-f4a4-437c-88fd-47308b6d2b79

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OVE Intervertebral fusion device with integrated fixation, cervical

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00889024329201

Customer Contacts

Device Sizes

Type Value Unit Text
Height 9 Millimeter
Width 12 Millimeter
Angle 0 degree
Length 14 Millimeter