Cure-aid® hydrocolloid dressings (Non-sterile) (UDI 06221329022311)
Manufactured by Pharmaplast
Device Regulatory Overview
The Cure-aid® hydrocolloid dressings (Non-sterile) (Model/Catalog Number: CFCNCOLLCPE50100) 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
- CFCNCOLLCPE50100
- Product Code / EMDN
- M04040301
- Device Name
- Hydrocolloid plasters
- Database Sync Date
- 2026-08-09 16:29:09
Full Regulatory Attributes
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{
"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® hydrocolloid dressings (Non-sterile)?
The registered manufacturer of record for Cure-aid® hydrocolloid dressings (Non-sterile) is Pharmaplast.
What is the Primary UDI-DI identifier for Cure-aid® hydrocolloid dressings (Non-sterile)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06221329022311.
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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