FDA UDI In Commercial Distribution 🇺🇸 United States

Dynesys®

DI: 00889024284012 · Model: 01.03756.455 · Zimmer GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
Dynesys®
Primary DI
00889024284012
Version / Model
01.03756.455
Company Name
Zimmer GmbH
Labeler DUNS
488133448
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2015-10-16
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
488d55dc-1868-4ed9-894d-6a0786eba112

Device Description

DYNESYS HA Pedicle+Set Screw 6.4x55

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NQP POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 00889024284012
Unit of Use 00889024407039

Customer Contacts

Device Sizes

Type Value Unit Text
Length 55 Millimeter
Outer Diameter 6.4 Millimeter