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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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H 600 — 14 UDI-DI variants, IVDR (Helmut Hund GmbH)

MD Atlas
Helmut Hund GmbH

Data from EUDAMED, last updated May 23, 2026

H 600

426074436H60035

14 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: 426074436H60035
Device name: H 600
Device model: Laboratory Microscope H 600
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jan 3, 2022

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

14 UDI-DI variants

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Applied filters

basicUdiUlid01FRFPRTKWB8GD0TF11SJXABKP

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

008.0387.004260744360242
008.0359.004260744360235
008.0384.004260744360228
008.0356.004260744360211
008.0371.004260744360280
008.0450.004260744360259
008.0450.G04260744360358
008.0365.004260744360174
008.0368.004260744360266
008.0353.004260744360204
008.0370.004260744360273
008.0414.004260744360198
008.0390.004260744360181
008.0380.004260744360167