FDA UDI In Commercial Distribution 🇺🇸 United States

APEX Knee System

DI: 00841690128632 · Model: KC-55121 · Omni Life Science, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
APEX Knee System
Primary DI
00841690128632
Version / Model
KC-55121
Catalog Number
KC-55121
Company Name
Omni Life Science, Inc.
Labeler DUNS
061339651
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-15
Public Version
3
Public Version Date
2021-09-13
Public Version Status
Update
Public Device Record Key
cb360765-5ed5-47e6-b707-f100da166b32

Device Description

Revision Fluted Stem 12mm x 100mm

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
Yes
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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
48066 Knee femur stem prosthesis

Identifiers

Type ID
Primary 00841690128632

Customer Contacts