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

MD Atlas
Wulff Med Tec GmbH

Data from EUDAMED, last updated May 23, 2026

MediMatt

40508244PWRUG

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: 40508244PWRUG
Device name: MediMatt
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 7, 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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Applied filters

basicUdiUlid01GRNPEER989MKYADDQMH263RK

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

4PWR2I100LS04050824261664
4PWRH1300LS04050824261695
4PWR61100LS04050824282003
4PWRG1200LS04050824284175
4PWR71100LS04050824276361
4PWR21100LS04050824261633
4PWRC1100LS04050824278532
4PWRE1400LS04050824282348
4PWR51100LS04050824271809
4PWRZ1100LS04050824282836
4PWRW1100LS04050824280238