FDA UDI In Commercial Distribution 🇺🇸 United States

Instrument Set

DI: 08033390025492 · Model: Impactor · LIMACORPORATE SPA
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Instrument Set
Primary DI
08033390025492
Version / Model
Impactor
Catalog Number
9056.10.020
Company Name
LIMACORPORATE SPA
Labeler DUNS
432066322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-27
Public Version
4
Public Version Date
2023-01-20
Public Version Status
Update
Public Device Record Key
cedd6d1d-2893-4552-aa15-af56172d5da4

Device Description

Impactor for Cemented Cups Dia.32mm - Acetabular Cup

Device Characteristics

Single Use
No
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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWZ Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer
KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

GMDN Terms

Code Name
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Primary 08033390025492

Premarket Submissions

Submission Number Supplement Number
K112158 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Dia.32mm