FDA UDI In Commercial Distribution 🇺🇸 United States

OMNI knee

DI: 00841690101062 · Model: KC-2204L · Omni Life Science, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OMNI knee
Primary DI
00841690101062
Version / Model
KC-2204L
Catalog Number
KC-2204L
Company Name
Omni Life Science, Inc.
Labeler DUNS
061339651
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-27
Public Version
5
Public Version Date
2021-10-01
Public Version Status
Update
Public Device Record Key
1ae03bd3-91c7-4d5e-8dc2-dbd39c5d4e22

Device Description

Primary Tibial Baseplate Cemented, size 4 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
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", "Radiation Sterilization"]

Product Codes

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

GMDN Terms

Code Name
32832 Uncoated knee tibia prosthesis, metallic

Identifiers

Type ID
Primary 00841690101062

Customer Contacts