eudamed_udi Primary ID: 00850053287091

Electrodo ReCure (UDI 00850053287091)

Manufactured by ANEUVO

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Electrodo ReCure (Model/Catalog Number: PAD-003) 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
Product Code / EMDN: Z120601
Device Name: ExaStim Stimulation System
Database Sync Date: 2026-08-09 16:29:22

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 Electrodo ReCure?

The registered manufacturer of record for Electrodo ReCure is ANEUVO.

What is the Primary UDI-DI identifier for Electrodo ReCure?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00850053287091.

What classification code is assigned to this device?

This device is registered under product classification code Z120601.

Similar Classification Devices (Z120601)

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