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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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Optical blood pressure measurement — 2 UDI-DI variants, MDR

MD Atlas
Effectum Medical AG

Data from EUDAMED, last updated May 23, 2026

Optical blood pressure measurement

764025502TD0123Y

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: Effectum Medical AG

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Device characteristics

Active deviceMeasuring function

Clinical investigations

Investigation number: NCT03875248
Registered: No
Countries: Switzerland

Identity & classification

Basic UDI-DI: 764025502TD0123Y
Device name: Optical blood pressure measurement
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Sep 20, 2023

Manufacturer & authorised representative

Manufacturer

Name: Effectum Medical AG
SRN: CH-MF-000012474
Country: Switzerland
Email: info@effectummedical.com
Phone: +41 77 493 72 72

Authorised representative

Name: MED-RAS GmbH Regulatory Affairs Service
SRN: DE-AR-000006211
Country: Germany
Phone: +49 4104 9944440

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HA74RJ4JYRYSK1T6QMNKRX6K

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

012.001.00107640255020618
012.001.00107640255020977