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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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medicus pro — 5 UDI-DI variants, IVDR (Helmut Hund GmbH)

MD Atlas
Helmut Hund GmbH

Data from EUDAMED, last updated May 23, 2026

medicus pro

426074436MEDPROAK

5 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Helmut Hund GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426074436MEDPROAK
Device name: medicus pro
Device model: Laboratory microscope medicus pro
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Dec 23, 2021

Manufacturer & authorised representative

Manufacturer

Name: Helmut Hund GmbH
SRN: DE-MF-000006335
Country: Germany
Email: j.haus@hund.de
Phone: +49 6441 20040

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01FQHDAWKKEK0A0YT03TFNCRWF

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

008.0460.004260744360099
008.0464.004260744360136
008.0462.004260744360112
008.0463.004260744360129
008.0461.004260744360105