FDA UDI In Commercial Distribution 🇺🇸 United States

APEX Knee System

DI: 00841690198413 · Model: KS-92110 · 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
00841690198413
Version / Model
KS-92110
Catalog Number
KS-92110
Company Name
Omni Life Science, Inc.
Labeler DUNS
061339651
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-10
Public Version
1
Public Version Date
2023-01-18
Public Version Status
New
Public Device Record Key
a410e65e-f9bf-47c7-b327-d885848f433b

Device Description

AK3 Ultra Insert Trial Size 1, 10mm

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
HWT TEMPLATE

GMDN Terms

Code Name
58716 Knee tibia prosthesis trial, reusable

Identifiers

Type ID
Primary 00841690198413

Customer Contacts