FDA UDI In Commercial Distribution 🇺🇸 United States

SMR Shoulder

DI: 08033390080637 · Model: 1360.50.820 · LIMACORPORATE SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
SMR Shoulder
Primary DI
08033390080637
Version / Model
1360.50.820
Catalog Number
1360.50.820
Company Name
LIMACORPORATE SPA
Labeler DUNS
432066322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-26
Public Version
1
Public Version Date
2024-08-05
Public Version Status
New
Public Device Record Key
f075ae0e-f963-434e-9410-4e4d3079adb4

Device Description

SMR Shoulder - Reverse liners 36mm (UHMWPE) +6mm

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

GMDN Terms

Code Name
48092 Polyethylene reverse shoulder prosthesis cup

Identifiers

Type ID
Primary 08033390080637

Premarket Submissions

Submission Number Supplement Number
K110598 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Dia 36mm #+6