eudamed_udi Primary ID: 00860003587164

ReCure® Electrode Pad (UDI 00860003587164)

Manufactured by ANEUVO

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The ReCure® Electrode Pad (Model/Catalog Number: PAD-003-02) is a medical device manufactured by ANEUVO. This product is indexed under FDA Product Code / Category Classification Z120601 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PAD-003-02
Product Code / EMDN: Z120601
Device Name: ExaStim Stimulation System
Database Sync Date: 2026-08-09 16:45:56

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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Frequently Asked Questions

Who is the primary manufacturer of ReCure® Electrode Pad?

The registered manufacturer of record for ReCure® Electrode Pad is ANEUVO.

What is the Primary UDI-DI identifier for ReCure® Electrode Pad?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00860003587164.

What classification code is assigned to this device?

This device is registered under product classification code Z120601.

Similar Classification Devices (Z120601)

Other Devices by ANEUVO

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