GUDIDData
gudid Primary ID: Cura RF Electrode Fixed 18-10s05FD

Curaway (UDI Cura RF Electrode Fixed 18-10s05FD)

Manufactured by Zhejiang CuraWay Medical Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Curaway - Primary ID Cura RF Electrode Fixed 18-10s05FD

Device Regulatory Overview

The Curaway (Model/Catalog Number: Cura RF Electrode Fixed 18-10s05FD) is a medical device manufactured by Zhejiang CuraWay Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification GEI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Cura RF Electrode Fixed 18-10s05FD
Product Code / EMDN
GEI
Device Name
Cura RF Electrode
Database Sync Date
2026-08-09 09:04:57

Full Regulatory Attributes

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Curaway?

The registered manufacturer of record for Curaway is Zhejiang CuraWay Medical Technology Co., Ltd..

What is the Primary UDI-DI identifier for Curaway?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Cura RF Electrode Fixed 18-10s05FD.

What classification code is assigned to this device?

This device is registered under product classification code GEI.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint