FDA UDI In Commercial Distribution 🇺🇸 United States

PRIMA

DI: 08033390201971 · Model: 1367.09.200 · LIMACORPORATE SPA
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PRIMA
Primary DI
08033390201971
Version / Model
1367.09.200
Catalog Number
1367.09.200
Company Name
LIMACORPORATE SPA
Labeler DUNS
432066322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-02-19
Public Version
1
Public Version Date
2026-02-27
Public Version Status
New
Public Device Record Key
12c640b6-b034-4714-9afd-08f366d7793c

Device Description

PRIMA - Reverse Insert # SHORT Dia. 40mm 0°Corr.

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

GMDN Terms

Code Name
60514 Metallic reverse shoulder prosthesis cup

Identifiers

Type ID
Primary 08033390201971

Premarket Submissions

Submission Number Supplement Number
K252352 000

Device Sizes

Type Value Unit Text
Device Size Text, specify # SHORT Dia. 40mm 0°Corr.