eudamed_udi
Primary ID: 06222023803473
Cure-Aid® Gentle (UDI 06222023803473)
Manufactured by Pharmaplast
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cure-Aid® Gentle - Primary ID 06222023803473
Device Regulatory Overview
The Cure-Aid® Gentle (Model/Catalog Number: CUREG60100) is a medical device manufactured by Pharmaplast. This product is indexed under FDA Product Code / Category Classification M04010101,M04010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CUREG60100
- Product Code / EMDN
- M04010101,M04010102
- Device Name
- Gentle Dressings
- Database Sync Date
- 2026-08-09 16:29:34
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® Gentle?
The registered manufacturer of record for Cure-Aid® Gentle is Pharmaplast.
What is the Primary UDI-DI identifier for Cure-Aid® Gentle?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06222023803473.
What classification code is assigned to this device?
This device is registered under product classification code M04010101,M04010102.
Similar Classification Devices (M04010101,M04010102)
Other Devices by Pharmaplast
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