FDA UDI In Commercial Distribution 🇺🇸 United States

OMNI K2 Hip

DI: 00841690102489 · Model: 130005 · Omni Life Science, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OMNI K2 Hip
Primary DI
00841690102489
Version / Model
130005
Catalog Number
130005
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
3
Public Version Date
2021-09-13
Public Version Status
Update
Public Device Record Key
d141cd6b-4855-4764-b409-55f2a18c985e

Device Description

K2 Femoral Stem, Size 5

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
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

GMDN Terms

Code Name
33581 Coated hip femur prosthesis, modular

Identifiers

Type ID
Primary 00841690102489

Customer Contacts