FDA UDI In Commercial Distribution 🇺🇸 United States

Trinica®

DI: 00889024324817 · Model: 07.01011.006 · ZIMMER SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trinica®
Primary DI
00889024324817
Version / Model
07.01011.006
Catalog Number
07.01011.006
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
5
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
88d20fd8-436f-464e-96e9-3e6d1287dde4

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

GMDN Terms

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

Identifiers

Type ID
Primary 00889024324817

Customer Contacts

Device Sizes

Type Value Unit Text
Angle 65 degree
Length 43 Millimeter