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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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CURVLIGHT — 4 UDI-DI variants, MDR (Wieth Medical Systems e.K.)

MD Atlas
Wieth Medical Systems e.K.

Data from EUDAMED, last updated May 23, 2026

CURVLIGHT

417000005028headlight5L

4 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: Wieth Medical Systems e.K.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 417000005028headlight5L
Device name: CURVLIGHT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 25, 2022

Manufacturer & authorised representative

Manufacturer

Name: Wieth Medical Systems e.K.
SRN: DE-MF-000019163
Country: Germany
Email: stephan.wieth@wieth-medical.de
Phone: +49 4121 7894370

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G3X62PH30FVCS4WHA8Q845TA

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

1013.0104170000273486
1011.0104170000050285
1012.0104170000273462
011010104170000273479