FDA UDI In Commercial Distribution 🇺🇸 United States

PointCloud

DI: TKRL0000LF225 · Model: UKI0101-L · Unik Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PointCloud
Primary DI
TKRL0000LF225
Version / Model
UKI0101-L
Company Name
Unik Orthopedics Inc.
Labeler DUNS
118205691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-22
Public Version
1
Public Version Date
2022-10-31
Public Version Status
New
Public Device Record Key
a225112e-0d7e-4090-981d-72e142685b08

Device Description

UNIKO PointCloud™ Knee Instrument Kit Left

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

GMDN Terms

Code Name
58910 Total knee prosthesis implantation guide-instrument kit

Identifiers

Type ID
Primary TKRL0000LF225

Premarket Submissions

Submission Number Supplement Number
K193312 000