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Dermaroller

EUDAMED

Class IIa (EU MDR)

Ref MC925Model MC402, MC405, MC410, MC415, MC420, MC425, MC902, MC905, MC910, MC915, MC920, MC925, MC1825,

by Dermaroller GmbH

Identity

Trade Name
Dermaroller EUDAMED
Device Name
Dermaroller MC / XCELLARISPRO MC EUDAMED
Model / Reference
MC402, MC405, MC410, MC415, MC420, MC425, MC902, MC905, MC910, MC915, MC920, MC925, MC1825, EUDAMED
MC925 EUDAMED

Identifiers

Primary DI / UDI-DI
04260446139252 EUDAMED
Basic UDI-DI
0426044613MCROLL001XV EUDAMED
EMDN Code
V901602 DERMOSURGERY INSTRUMENTS AND KITS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Dermaroller by Dermaroller GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Dermaroller GmbH
EUDAMED SRN
DE-MF-000005021

Sources (1)

  • EUDAMED cbaf2145-42ae-4642-9003-86982c7515dd 61 fields · synced May 23, 2026