FDA UDI In Commercial Distribution 🇺🇸 United States

Dynesys

DI: 00880304989375 · Model: 07.00766.701 · ZIMMER SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Dynesys
Primary DI
00880304989375
Version / Model
07.00766.701
Catalog Number
07.00766.701
Company Name
ZIMMER SPINE, INC.
Labeler DUNS
787663400
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-30
Public Version
3
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
7ac1b77a-5ff9-4fb4-bdcb-33d3b826055b

Device Description

Dynesys® TL Cord Tensioner with Ratchet

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
NQP Posterior Metal/Polymer Spinal System, Fusion

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 00880304989375

Customer Contacts