FDA UDI In Commercial Distribution 🇺🇸 United States

EXULT Knee Replacement System

DI: 08800068940865 · Model: KA.ICR.0211-PPX · Corentec Co., Ltd
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EXULT Knee Replacement System
Primary DI
08800068940865
Version / Model
KA.ICR.0211-PPX
Company Name
Corentec Co., Ltd
Labeler DUNS
688739895
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-22
Public Version
3
Public Version Date
2022-03-22
Public Version Status
Update
Public Device Record Key
91d45317-77f0-424a-939a-413eb72b4bbc

Device Description

Tibial Insert Trial CR #02 T11

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

Product Codes

Code Name
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer

GMDN Terms

Code Name
58716 Knee tibia prosthesis trial, reusable

Identifiers

Type ID
Primary 08800068940865

Customer Contacts

Phone
+82414107176