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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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PureMotion — 4 UDI-DI variants, MDR (medentex GmbH)

MD Atlas
medentex GmbH

Data from EUDAMED, last updated May 23, 2026

PureMotion

426071187-PureMotion-HZ

4 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: medentex GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426071187-PureMotion-HZ
Device name: PureMotion
Device model: PureMotion
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 2, 2026

Manufacturer & authorised representative

Manufacturer

Name: medentex GmbH
SRN: DE-MF-000005860
Country: Germany
Email: info@medentex.de
Phone: +49 (0)5205 7516 0

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KGF2C8G2C6TG6PZ5ZP1HHCRB

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

A000023504260711872358
A000024604260711872464
A000017904260711871795
A000025104260711872518