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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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CoMoveIT Flex — 3 UDI-DI variants, MDR (CoMoveIT)

MD Atlas
CoMoveIT

Data from EUDAMED, last updated May 23, 2026

CoMoveIT Flex

5430002911CMFLEXP2

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: CoMoveIT

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5430002911CMFLEXP2
Device name: CoMoveIT Flex
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: CoMoveIT
SRN: BE-MF-000017867
Country: Belgium
Email: info@comoveit.com
Phone: +32477880175

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KJWJZYK3ZHQ9AH6SJHA7C8YW

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

CoMoveIT Flex Footpad05430002911113
CoMoveIT Flex05430002911106
CoMoveIT Flex dF05430002911137