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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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clinalytix — 5 UDI-DI variants, MDR (DH Healthcare GmbH)

MD Atlas
DH Healthcare GmbH

Data from EUDAMED, last updated May 23, 2026

clinalytix

426069399CLINALYTIXH4

5 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: DH Healthcare GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426069399CLINALYTIXH4
Device name: clinalytix
Device model: clinalytix
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 4, 2022

Manufacturer & authorised representative

Manufacturer

Name: DH Healthcare GmbH
SRN: DE-MF-000009069
Country: Germany
Email: healthcare.de@dedalus-group.com
Phone: +49 228 2668 000

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G68H0WXPXMFY1S4ZGXPHCEYX

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

clinalytix Medical A04260693990101
clinalytix04260693990095
clinalytix04260693990033
clinalytix Medical AI04260693990149
clinalytix Medical AI04260693990118