FDA UDI In Commercial Distribution 🇺🇸 United States

SMR System

DI: 08033390272568 · Model: 1352.15.010 · LIMACORPORATE SPA
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SMR System
Primary DI
08033390272568
Version / Model
1352.15.010
Catalog Number
1352.15.010
Company Name
LIMACORPORATE SPA
Labeler DUNS
432066322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-22
Public Version
1
Public Version Date
2024-03-01
Public Version Status
New
Public Device Record Key
ec01022d-2c6d-487c-8e3d-742dad30fcd2

Device Description

SMR System - Humeral Body Reverse

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
KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
PHX Shoulder Prosthesis, Reverse Configuration

GMDN Terms

Code Name
60511 Reverse shoulder prosthesis body

Identifiers

Type ID
Primary 08033390272568

Premarket Submissions

Submission Number Supplement Number
K110598 000