FDA UDI In Commercial Distribution 🇺🇸 United States

Omnifit

DI: 07613327101232 · Model: 2041C-2250 · Howmedica Osteonics Corp.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Omnifit
Primary DI
07613327101232
Version / Model
2041C-2250
Catalog Number
2041C-2250
Company Name
Howmedica Osteonics Corp.
Labeler DUNS
058311945
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
31d4878a-a15b-43d0-bc1d-acaa469946a3

Device Description

10 Degree Series II Insert

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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LWJ Prosthesis, hip, semi-constrained, metal/polymer, uncemented
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

GMDN Terms

Code Name
43168 Non-constrained polyethylene acetabular liner

Identifiers

Type ID
Primary 07613327101232

Premarket Submissions

Submission Number Supplement Number
K974685 000

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 22.0 Millimeter