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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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mediCAD® — 2 UDI-DI variants, MDR (mediCAD Hectec GmbH)

MD Atlas
mediCAD Hectec GmbH

Data from EUDAMED, last updated May 23, 2026

mediCAD®

426048972MCADBW

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: mediCAD Hectec GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 426048972MCADBW
Device name: mediCAD®
Device model: Medical Software
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 9, 2022

Manufacturer & authorised representative

Manufacturer

Name: mediCAD Hectec GmbH
SRN: DE-MF-000006987
Country: Germany
Email: info@medicad.eu
Phone: +49 871 330 203 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G3XGP7AF1QHP35P3CBSM81XA

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

medc-10104260489720110
mediCAD® Web04260489720202