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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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VarioMatt — 2 UDI-DI variants, MDR (Wulff Med Tec GmbH)

MD Atlas
Wulff Med Tec GmbH

Data from EUDAMED, last updated May 23, 2026

VarioMatt

4050824WBMPYN

2 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: Wulff Med Tec GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4050824WBMPYN
Device name: VarioMatt
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 29, 2023

Manufacturer & authorised representative

Manufacturer

Name: Wulff Med Tec GmbH
SRN: DE-MF-000010006
Country: Germany
Email: info@wulff-med.de
Phone: +49 4836996410

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01H8ZXE1CGD4TJC74RRETVGBV6

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

WB-59-0171-000004050824262395
WB-50-0940-000004050824263453