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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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MH Guide — 2 UDI-DI variants, IVDR (Molecular Health GmbH)

MD Atlas
Molecular Health GmbH

Data from EUDAMED, last updated May 23, 2026

MH Guide

4260563550237VS

2 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Manufacturer: Molecular Health GmbH

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 4260563550237VS
Device name: MH Guide
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Special device type: refdata.special-ivd-device-type.software
Version date: Aug 1, 2022

Manufacturer & authorised representative

Manufacturer

Name: Molecular Health GmbH
SRN: DE-MF-000012861
Country: Germany
Email: niels.bojunga@molecularhealth.com
Phone: +4915153850196

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FPA7Q6CQBBRS7Z5V76MMKSCG

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

MH Guide04260563550343
MH Guide04260563550350