FDA UDI In Commercial Distribution 🇺🇸 United States

SMR Shoulder

DI: 08033390106436 · Model: Bone Graft Instrument Set · LIMACORPORATE SPA
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SMR Shoulder
Primary DI
08033390106436
Version / Model
Bone Graft Instrument Set
Catalog Number
9013.75.465
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
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
d18f2aed-a678-4b6b-96e7-dcd8b91c7a92

Device Description

Bone Graft Instrument Set - STD Graft Reamer

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

GMDN Terms

Code Name
60927 Glenoid orthopaedic reamer

Identifiers

Type ID
Primary 08033390106436

Premarket Submissions

Submission Number Supplement Number
K161120 000

Device Sizes

Type Value Unit Text
Device Size Text, specify STD