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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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Dicompass — 2 UDI-DI variants, MDR (MEDORO s.r.o.)

MD Atlas
MEDORO s.r.o.

Data from EUDAMED, last updated May 23, 2026

Dicompass

859421232DICOMPASSGM

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: MEDORO s.r.o.

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Device characteristics

Active deviceMeasuring function

Legacy certificates

Certificate number: 2022-MDR/QS-020
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: 3EC International a.s. (2265)
Validity: Mar 19, 2025 → Sep 9, 2027

Identity & classification

Basic UDI-DI: 859421232DICOMPASSGM
Device name: Dicompass
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Jul 22, 2025

Manufacturer & authorised representative

Manufacturer

Name: MEDORO s.r.o.
SRN: CZ-MF-000024306
Country: Czechia
Email: info@medoro.org
Phone: +420775324005

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K0RQSYEEJTR03SAS31Y5CSZE

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

208594212320022
108594212320015