eudamed_udi
Primary ID: 06221329018635
Cure-Aid® Foot Care Plasters (Non-Sterile) (UDI 06221329018635)
Manufactured by Pharmaplast
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cure-Aid® Foot Care Plasters (Non-Sterile) - Primary ID 06221329018635
Device Regulatory Overview
The Cure-Aid® Foot Care Plasters (Non-Sterile) (Model/Catalog Number: CFCNCOLLTPU2852) is a medical device manufactured by Pharmaplast. This product is indexed under FDA Product Code / Category Classification M04040301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CFCNCOLLTPU2852
- Product Code / EMDN
- M04040301
- Device Name
- Hydrocolloid plasters
- Database Sync Date
- 2026-08-09 16:29:13
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® Foot Care Plasters (Non-Sterile)?
The registered manufacturer of record for Cure-Aid® Foot Care Plasters (Non-Sterile) is Pharmaplast.
What is the Primary UDI-DI identifier for Cure-Aid® Foot Care Plasters (Non-Sterile)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06221329018635.
What classification code is assigned to this device?
This device is registered under product classification code M04040301.
Similar Classification Devices (M04040301)
Other Devices by Pharmaplast
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