FDA UDI In Commercial Distribution 🇺🇸 United States

SMR Shoulder

DI: 08033390108782 · Model: Bone Graft Instrument Set · LIMACORPORATE SPA
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
SMR Shoulder
Primary DI
08033390108782
Version / Model
Bone Graft Instrument Set
Catalog Number
9013.75.438
Company Name
LIMACORPORATE SPA
Labeler DUNS
432066322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-25
Public Version
5
Public Version Date
2023-08-01
Public Version Status
Update
Public Device Record Key
b3a8c176-3b2e-4006-9bea-8138d8a1adcf

Device Description

Bone Graft Instrument Set - Head K-Wire Positioner

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

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 08033390108782

Premarket Submissions

Submission Number Supplement Number
K161120 000