FDA UDI In Commercial Distribution 🇺🇸 United States

Revision Femoral Head

DI: 08033390297820 · Model: 5010.42.032 · LIMACORPORATE SPA
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Revision Femoral Head
Primary DI
08033390297820
Version / Model
5010.42.032
Catalog Number
5010.42.032
Company Name
LIMACORPORATE SPA
Labeler DUNS
432066322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-27
Public Version
1
Public Version Date
2025-11-04
Public Version Status
New
Public Device Record Key
ce1f4a55-6445-4c76-b989-9c45a8c52454

Device Description

Revision Femoral Head - Dia.32mm Medium Taper 12/14

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

GMDN Terms

Code Name
38156 Ceramic femoral head prosthesis

Identifiers

Type ID
Primary 08033390297820

Premarket Submissions

Submission Number Supplement Number
K243809 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Dia.32mm Medium Taper 12/14