eudamed_udi
Primary ID: 06221329002474
Cure-Aid® Scar Reduction (UDI 06221329002474)
Manufactured by Pharmaplast
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cure-Aid® Scar Reduction - Primary ID 06221329002474
Device Regulatory Overview
The Cure-Aid® Scar Reduction (Model/Catalog Number: CURESISPOT2) is a medical device manufactured by Pharmaplast. This product is indexed under FDA Product Code / Category Classification M04040701 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CURESISPOT2
- Product Code / EMDN
- M04040701
- Device Name
- Scar reduction dressings
- Database Sync Date
- 2026-08-09 16:30:41
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® Scar Reduction?
The registered manufacturer of record for Cure-Aid® Scar Reduction is Pharmaplast.
What is the Primary UDI-DI identifier for Cure-Aid® Scar Reduction?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06221329002474.
What classification code is assigned to this device?
This device is registered under product classification code M04040701.
Similar Classification Devices (M04040701)
Other Devices by Pharmaplast
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