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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 neo — 3 UDI-DI variants, IVDR (Helmut Hund GmbH)

MD Atlas
Helmut Hund GmbH

Data from EUDAMED, last updated May 23, 2026

medicus neo

426074436medicusneoFJ

3 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

Professional testing

Identity & classification

Basic UDI-DI: 426074436medicusneoFJ
Device name: medicus neo
Device model: Laboratory Microscopy
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Nov 10, 2025

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

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K9PKNT9PNCZ559Y3SS40VZD2

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

008.0470.004260744360372
008.0471.004260744360389
008.0472.004260744360396