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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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Blue light radiometer — 5 UDI-DI variants, MDR (Derungs Licht AG)

MD Atlas
Derungs Licht AG

Data from EUDAMED, last updated May 23, 2026

Blue light radiometer

76401587148Y

5 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: Derungs Licht AG

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 76401587148Y
Device name: Blue light radiometer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 25, 2024

Manufacturer & authorised representative

Manufacturer

Name: Derungs Licht AG
SRN: CH-MF-000015827
Country: Switzerland
Email: mailbox@derungs.swiss

Authorised representative

Name: Derungs Medical GmbH
SRN: DE-AR-000033841
Country: Germany
Phone: +49-7731-909717-0

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

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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

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