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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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wiroLIGHT PF — 27 UDI-DI variants, MDR (WIROS Wilfried Rosbach GmbH)

MD Atlas
WIROS Wilfried Rosbach GmbH

Data from EUDAMED, last updated May 23, 2026

wiroLIGHT PF

4051642-wiroLIGHTPF-22

27 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: WIROS Wilfried Rosbach GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4051642-wiroLIGHTPF-22
Device name: wiroLIGHT PF
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 31, 2026

Manufacturer & authorised representative

Manufacturer

Name: WIROS Wilfried Rosbach GmbH
SRN: DE-MF-000004956
Country: Germany
Email: michael.hummels@wiros.de
Phone: +49 (0) 2154 89 141 0

Variants by status

UDI-DI variants

27 UDI-DI variants

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Applied filters

basicUdiUlid01KN1CH9ZN7QE17458S1N1VHXW

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

No registered UDI-DI variants for this device family.