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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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Dermaroller MC / XCELLARISPRO MC — 13 UDI-DI variants, MDR

MD Atlas
Dermaroller GmbH

Data from EUDAMED, last updated May 23, 2026

Dermaroller MC / XCELLARISPRO MC

0426044613MCROLL001XV

13 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Dermaroller GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0426044613MCROLL001XV
Device name: Dermaroller MC / XCELLARISPRO MC
Device model: MC402, MC405, MC410, MC415, MC420, MC425, MC902, MC905, MC910, MC915, MC920, MC925, MC1825,
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 16, 2023

Manufacturer & authorised representative

Manufacturer

Name: Dermaroller GmbH
SRN: DE-MF-000005021
Country: Germany
Email: regaffairs@dermaroller.com
Phone: +49 (0) 5331 710 8480

Variants by status

UDI-DI variants

13 UDI-DI variants

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Applied filters

basicUdiUlid01GPX4TZJW6Q83H91NWZSTNCJF

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

MC90204260446139023
MC92004260446139207
MC90504260446139054
MC91004260446139108
MC41004260446134103
MC42504260446134257
MC182504260446131805
MC40504260446134059
MC41504260446134158
MC91504260446139153
MC42004260446134202
MC92504260446139252
MC40204260446134028