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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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EPS Madrid lábfej tehermentesítő cipő — 5 UDI-DI variants, MDR

MD Atlas
Ergo-Prevent Kft.

Data from EUDAMED, last updated May 24, 2026

EPS Madrid lábfej tehermentesítő cipő

5999884370madrid5X

5 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Ergo-Prevent Kft.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5999884370madrid5X
Device name: EPS Madrid lábfej tehermentesítő cipő
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 27, 2024

Manufacturer & authorised representative

Manufacturer

Name: Ergo-Prevent Kft.
SRN: HU-MF-000042772
Country: Hungary
Email: info@ergoprevent.hu
Phone: +36 30-641-41-20

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01J6A8596WH4QGYDZ463NJT7C0

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

599988437008605999884370086
599988437007905999884370079
599988437009305999884370093
599988437005505999884370055
599988437006205999884370062