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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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EMALED200D — 3 UDI-DI variants, MDR (EMA-LED GmbH)

MD Atlas
EMA-LED GmbH

Data from EUDAMED, last updated May 23, 2026

EMALED200D

426025797EMALEDLIGHTPY

3 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: EMA-LED GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426025797EMALEDLIGHTPY
Device name: EMALED200D
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: EMA-LED GmbH
SRN: DE-MF-000017063
Country: Germany
Email: info@emaled.de
Phone: +49 6022 206 811

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KRAZRCK6PBBR7MEBZWYNWRHG

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

EMALED200D04260257971935
EMALED200W04260257972048
EMALED200D+04260257972130