FDA UDI In Commercial Distribution 🇺🇸 United States

SIDEKICK

DI: 00840420128768 · Model: RRCF0160 · WRIGHT MEDICAL TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SIDEKICK
Primary DI
00840420128768
Version / Model
RRCF0160
Catalog Number
RRCF0160
Company Name
WRIGHT MEDICAL TECHNOLOGY, INC.
Labeler DUNS
807201207
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-01
Public Version
4
Public Version Date
2022-03-24
Public Version Status
Update
Public Device Record Key
96bb13af-7370-479a-8711-7d1a5f0354f5

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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

GMDN Terms

Code Name
35647 External orthopaedic fixation system, reusable

Identifiers

Type ID
Primary 00840420128768

Customer Contacts

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 160 Millimeter
Device Size Text, specify Circular
Device Size Text, specify Size: 160mm