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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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MEDPRO FLEX — 4 UDI-DI variants, MDR (Exportex Iwona Irzyk)

MD Atlas
Exportex Iwona Irzyk

Data from EUDAMED, last updated May 30, 2026

MEDPRO FLEX

5902003786MEDPROFLEXCV

4 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: Exportex Iwona Irzyk

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5902003786MEDPROFLEXCV
Device name: MEDPRO FLEX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: Exportex Iwona Irzyk
SRN: PL-MF-000047484
Country: Poland
Email: exportex.pl@gmail.com
Phone: +48500834384

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KC54M53QHCEB7KYE5TD5AWT4

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

705902003786064
605902003786057
905902003786095
805902003786071