FDA UDI In Commercial Distribution 🇺🇸 United States

ProMade

DI: 08033390237420 · Model: 9CC0.13.03E · LIMACORPORATE SPA
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ProMade
Primary DI
08033390237420
Version / Model
9CC0.13.03E
Catalog Number
9CC0.13.03E
Company Name
LIMACORPORATE SPA
Labeler DUNS
432066322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-21
Public Version
2
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
89c51732-946e-4cfe-97f0-f33a374405bc

Device Description

M8 Long Handle

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
KWT Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented
HSD Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 08033390237420

Premarket Submissions

Submission Number Supplement Number
K100858 000