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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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MasterScope — 11 UDI-DI variants, MDR (eResearchTechnology GmbH)

MD Atlas
eResearchTechnology GmbH

Data from EUDAMED, last updated May 23, 2026

MasterScope

4057155Z12150101001C3

11 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: eResearchTechnology GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4057155Z12150101001C3
Device name: MasterScope
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 11, 2023

Manufacturer & authorised representative

Manufacturer

Name: eResearchTechnology GmbH
SRN: DE-MF-000008015
Country: Germany
Email: customercare@clario.com
Phone: +49 9 305 720 9891

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H02F8P9MZTMX0H3G6Y4D49DN

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

1714xx + 99312504057155000030
171400, 17141004057155000023
70623504057155000061
17160004057155000610
17160104057155000627
MasterScope ECG04057155000054
MasterScope WSSU04057155000566
17161004057155000634
17161104057155000641
70955404057155000078
70955504057155000368