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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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Wound Plasters — 7 UDI-DI variants, MDR

MD Atlas
CMC Consumer Medical Care GmbH

Data from EUDAMED, last updated May 23, 2026

Wound Plasters

40424414299HU

7 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: CMC Consumer Medical Care GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40424414299HU
Device name: Wound Plasters
Device model: 4299
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: CMC Consumer Medical Care GmbH
SRN: DE-MF-000006178
Country: Germany
Email: registrations@cmc-group.de
Phone: +49 7325 9244 0

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KR0ER2GWE8KGD8XADSDV9H5P

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

53329604042441024128
53329704042441024135
53330704042441024142
my patch BY Cosmoplast ANIMAL PLASTERS ELASTIC04046871012823
my patch BY Cosmoplast FUNNY PLASTERS WATER RESISTANT04046871012946
my patch BY Cosmoplast GLITTER PLASTERS WATERPROOF04046871012861
my patch BY Cosmoplast KAWAII PLASTERS SENSITIVE04046871012908