FDA UDI In Commercial Distribution 🇺🇸 United States

OMNI Hip

DI: 00841690119456 · Model: H3-82243 · Omni Life Science, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OMNI Hip
Primary DI
00841690119456
Version / Model
H3-82243
Catalog Number
H3-82243
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
4
Public Version Date
2021-09-13
Public Version Status
Update
Public Device Record Key
53ea01b0-6b9b-49b6-b247-2fb8fc452db1

Device Description

Bipolar Head, 43mm OD, 22.225mm ID

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
KWY Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented

GMDN Terms

Code Name
33695 Bipolar femoral head outer component, hemiarthroplasty

Identifiers

Type ID
Primary 00841690119456

Customer Contacts