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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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EUROPROBE — 34 UDI-DI variants, MDR (EURORAD 2-6)

MD Atlas
EURORAD 2-6

Data from EUDAMED, last updated May 19, 2026

EUROPROBE

37005422000000EUROPROBEKJ

34 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: EURORAD 2-6

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 37005422000000EUROPROBEKJ
Device name: EUROPROBE
Device model: EUROPROBE 3.2
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 13, 2023

Manufacturer & authorised representative

Manufacturer

Name: EURORAD 2-6
SRN: FR-MF-000000156
Country: France
Email: info@eurorad.com
Phone: +33 3 88 26 81 30

Variants by status

UDI-DI variants

34 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HHEWVZZ9PEA121WBBRT89GA4

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

SOE3216-AC03700542200339
SOE3216-7-AC03700542200377
SOE3216-BT03700542200551
SOE3211-1403700542200407
SOE3211-14-AC03700542200414
SOE3216-7-D03700542200384
SOE3211-D-AC03700542200315
SOE3211-14-D-AC03700542200438
EUROPROBE 3.2 MODULE03700542200254

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