eudamed_udi
Primary ID: 06221329013319
Cure-Aid® Corn removal plasters (UDI 06221329013319)
Manufactured by Pharmaplast
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cure-Aid® Corn removal plasters - Primary ID 06221329013319
Device Regulatory Overview
The Cure-Aid® Corn removal plasters (Model/Catalog Number: CSANCORPLRF2045) is a medical device manufactured by Pharmaplast. This product is indexed under FDA Product Code / Category Classification M0412 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CSANCORPLRF2045
- Product Code / EMDN
- M0412
- Device Name
- Corn, callus and wart removal dressings
- Database Sync Date
- 2026-08-09 16:29:08
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Cure-Aid® Corn removal plasters?
The registered manufacturer of record for Cure-Aid® Corn removal plasters is Pharmaplast.
What is the Primary UDI-DI identifier for Cure-Aid® Corn removal plasters?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06221329013319.
What classification code is assigned to this device?
This device is registered under product classification code M0412.
Similar Classification Devices (M0412)
Other Devices by Pharmaplast
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