eudamed_udi Primary ID: 08437013961592

REAL MIDI SYSTEM TOTAL FIX (UDI 08437013961592)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The REAL MIDI SYSTEM TOTAL FIX (Model/Catalog Number: RPP9010MD) is a medical device manufactured by DURVIZ, S.L.. This product is indexed under FDA Product Code / Category Classification W0104050199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: RPP9010MD
Product Code / EMDN: W0104050199
Device Name: REAL MIDI SYSTEM- SISTEMA DE TRANSPORTE, CONSERVACIÓN Y CONCENTRACIÓN DE PARÁSITOS EN HECES
Database Sync Date: 2026-08-09 16:47:08

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 REAL MIDI SYSTEM TOTAL FIX?

The registered manufacturer of record for REAL MIDI SYSTEM TOTAL FIX is DURVIZ, S.L..

What is the Primary UDI-DI identifier for REAL MIDI SYSTEM TOTAL FIX?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08437013961592.

What classification code is assigned to this device?

This device is registered under product classification code W0104050199.

Similar Classification Devices (W0104050199)

Other Devices by DURVIZ, S.L.

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