FDA UDI In Commercial Distribution 🇺🇸 United States

KinematX

DI: 00842078112090 · Model: 137-31000-S · EXTREMITY MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KinematX
Primary DI
00842078112090
Version / Model
137-31000-S
Company Name
EXTREMITY MEDICAL, LLC
Labeler DUNS
832720358
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-27
Public Version
1
Public Version Date
2020-11-04
Public Version Status
New
Public Device Record Key
9a57e65e-3ec1-46c9-8240-313bcdf43ef0

Device Description

Carpal Cap; Sterile Packed

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
JWJ Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained

GMDN Terms

Code Name
33705 Total wrist prosthesis

Identifiers

Type ID
Primary 00842078112090

Premarket Submissions

Submission Number Supplement Number
K191525 000