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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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Hand-held examination light — 6 UDI-DI variants, MDR

MD Atlas
Derungs Licht AG

Data from EUDAMED, last updated May 23, 2026

Hand-held examination light

763079512SB

6 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 device

Identity & classification

Basic UDI-DI: 763079512SB
Device name: Hand-held examination light
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 25, 2026

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

6 UDI-DI variants

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Applied filters

basicUdiUlid01G6QXAEBW1N4R3BN8T4NV5NP6

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

OPTICLUX Hand 10-1 DL07640158711477
OPTICLUX Hand 10-1 DL Bundle07640158713013
OPTICLUX Hand 10-2 UV07640158711484
OPTICLUX Hand 10-2 UV Bundle07640158713020
Opticlux hand DL07640158711248
Opticlux hand UV07640158711255