FDA UDI In Commercial Distribution 🇺🇸 United States

Vitality®

DI: 00889024010642 · Model: 07.02128.001 · ZIMMER SPINE, INC.
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vitality®
Primary DI
00889024010642
Version / Model
07.02128.001
Catalog Number
07.02128.001
Company Name
ZIMMER SPINE, INC.
Labeler DUNS
787663400
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-27
Public Version
4
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
8cf8bdbb-fcf8-46ba-affb-2e3215f5fc86

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
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
OSH Pedicle screw spinal system, adolescent idiopathic scoliosis
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
MNH Orthosis, spondylolisthesis spinal fixation
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease

GMDN Terms

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

Identifiers

Type ID
Primary 00889024010642

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify SIZE 27 TORX