FDA UDI In Commercial Distribution 🇺🇸 United States

SLK Evo

DI: 05051693400023 · Model: CR Femoral (STD) Right 60mm · IMPLANTS INTERNATIONAL LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SLK Evo
Primary DI
05051693400023
Version / Model
CR Femoral (STD) Right 60mm
Catalog Number
KS5961
Company Name
IMPLANTS INTERNATIONAL LTD
Labeler DUNS
346627222
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-31
Public Version
3
Public Version Date
2019-12-11
Public Version Status
Update
Public Device Record Key
3c11e12a-8ff5-4a98-8985-3d7d408a682a

Device Description

Cruciate Retaining Femoral Componant for Cemented applications (Cobalt Chrome), Denoted size 60mm (Width) Anatomical Orientation - Right

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
MR Conditional
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

Code Name
32831 Uncoated knee femur prosthesis, metallic

Identifiers

Type ID
Primary 05051693400023

Customer Contacts

Device Sizes

Type Value Unit Text
Width 60 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Room temperature and Dry