eudamed_udi Primary ID: 08033638321744

electra 4 (UDI 08033638321744)

Manufactured by LED SpA

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

Scannable UDI-DI Representation

Device Regulatory Overview

The electra 4 (Model/Catalog Number: ELC004) is a medical device manufactured by LED SpA. This product is indexed under FDA Product Code / Category Classification Z120601 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ELC004
Product Code / EMDN: Z120601
Device Name: electra 4
Database Sync Date: 2026-08-09 17:00:05

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 electra 4?

The registered manufacturer of record for electra 4 is LED SpA.

What is the Primary UDI-DI identifier for electra 4?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033638321744.

What classification code is assigned to this device?

This device is registered under product classification code Z120601.

Similar Classification Devices (Z120601)

Other Devices by LED SpA

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