GUDIDData
eudamed_udi Primary ID: 06958066424046

Patch ECG Electrode (UDI 06958066424046)

Manufactured by Suzhou Beneware Medical Equipment Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Patch ECG Electrode - Primary ID 06958066424046

Device Regulatory Overview

The Patch ECG Electrode (Model/Catalog Number: EL-03A-EN) is a medical device manufactured by Suzhou Beneware Medical Equipment Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification C020501 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
EL-03A-EN
Product Code / EMDN
C020501
Device Name
Patch ECG Electrode
Database Sync Date
2026-08-09 16:30:32

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 Patch ECG Electrode?

The registered manufacturer of record for Patch ECG Electrode is Suzhou Beneware Medical Equipment Co.,Ltd..

What is the Primary UDI-DI identifier for Patch ECG Electrode?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06958066424046.

What classification code is assigned to this device?

This device is registered under product classification code C020501.

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