GUDIDData
eudamed_udi Primary ID: 06221329011360

Cure-Aid® Manuka Hydrogel Bandages (Non-Sterile) (UDI 06221329011360)

Manufactured by Pharmaplast

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cure-Aid® Manuka Hydrogel Bandages (Non-Sterile) - Primary ID 06221329011360

Device Regulatory Overview

The Cure-Aid® Manuka Hydrogel Bandages (Non-Sterile) (Model/Catalog Number: CUREMGELN4560) is a medical device manufactured by Pharmaplast. This product is indexed under FDA Product Code / Category Classification M04040501,M04040502 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CUREMGELN4560
Product Code / EMDN
M04040501,M04040502
Device Name
Hydrogel dressings [Cure-Aid® Hydrogel Bandages (Sterile and Non-Sterile), Cure-Aid® Aloe Vera Hydrogel Bandages (Sterile and Non-Sterile) and Cure-Aid® Manuka Hydrogel Bandages (Sterile and Non-Sterile)]
Database Sync Date
2026-08-09 16:28:59

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Cure-Aid® Manuka Hydrogel Bandages (Non-Sterile)?

The registered manufacturer of record for Cure-Aid® Manuka Hydrogel Bandages (Non-Sterile) is Pharmaplast.

What is the Primary UDI-DI identifier for Cure-Aid® Manuka Hydrogel Bandages (Non-Sterile)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06221329011360.

What classification code is assigned to this device?

This device is registered under product classification code M04040501,M04040502.

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