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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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ViskoMatt — 11 UDI-DI variants, MDR (Wulff Med Tec GmbH)

MD Atlas
Wulff Med Tec GmbH

Data from EUDAMED, last updated May 23, 2026

ViskoMatt

4050824WBQQ

11 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: 4050824WBQQ
Device name: ViskoMatt
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 28, 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

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H8XYKNKS0ZRPSFM0TC0FGP4B

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-50-068004050824263996
WB-59-014704050824265075
WB-50-066904050824234590
WB-50-080104050824263804
WB-50-067004050824263330
WB-50-087904050824264023
WB-59-014304050824256660
WB-50-070104050824262333
WB-50-082404050824264955
WB-59-016504050824263231
WB-59-012004050824263361