FDA UDI In Commercial Distribution 🇺🇸 United States

Versa-Fx®

DI: 00889024035652 · Model: 1193-05-27 · Zimmer, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Versa-Fx®
Primary DI
00889024035652
Version / Model
1193-05-27
Catalog Number
00-1193-005-27
Company Name
Zimmer, Inc.
Labeler DUNS
056038268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-17
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
d56002a5-8969-409d-bbde-25c9373e5d4d

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
JDO DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT
KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

GMDN Terms

Code Name
46646 Orthopaedic bone screw, non-bioabsorbable, sterile

Identifiers

Type ID
Primary 00889024035652

Customer Contacts

Device Sizes

Type Value Unit Text
Length 70 Millimeter
Device Size Text, specify 12.7 mm Thread Diameter