FDA UDI In Commercial Distribution 🇺🇸 United States

PRIMA TT Glenoid

DI: 08033390273930 · Model: 9019.75.302 · LIMACORPORATE SPA
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
PRIMA TT Glenoid
Primary DI
08033390273930
Version / Model
9019.75.302
Catalog Number
9019.75.302
Company Name
LIMACORPORATE SPA
Labeler DUNS
432066322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-10
Public Version
1
Public Version Date
2024-05-20
Public Version Status
New
Public Device Record Key
62e09adf-ecf7-4671-99ca-122fa8f32e58

Device Description

PRIMA TT Glenoid - K-Wire Positioning Jig Dia. 28 mm Regular

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
PHX Shoulder Prosthesis, Reverse Configuration
MBF Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 08033390273930

Device Sizes

Type Value Unit Text
Device Size Text, specify Dia. 28 mm Regular