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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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M-Medikation — 2 UDI-DI variants, MDR (Meierhofer Medizintechnik GmbH)

MD Atlas
Meierhofer Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

M-Medikation

426235228M-MedikationJ8

2 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: Meierhofer Medizintechnik GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426235228M-MedikationJ8
Device name: M-Medikation
Device model: 4.x.x
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Apr 15, 2024

Manufacturer & authorised representative

Manufacturer

Name: Meierhofer Medizintechnik GmbH
SRN: DE-MF-000008662
Country: Germany
Email: info@meierhofer.com
Phone: +49894423160

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01H0J52CMK56EW311RQ5MPKHMG

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

no04262352280059
no04262352280080