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Dermlite

EUDAMED

Class I (EU MDR)

Ref DSP

by DermLite LLC

Identity

Trade Name
DERMLITE EUDAMED
Device Name
DL200/Lumio S Drawstring Pouch EUDAMED
Model / Reference
DSP EUDAMED

Identifiers

Primary DI / UDI-DI
08500176510744 EUDAMED
Basic UDI-DI
0850017651074SP EUDAMED
EMDN Code
Z12040108 DERMATOSCOPES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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

Dermlite by DermLite LLC — Class I — 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
DermLite LLC
EUDAMED SRN
US-MF-000005170
Authorised Representative
E C REP LIMITED IE-AR-000003995

Sources (1)

  • EUDAMED 82eff05e-dc04-4943-8653-7344d46fd681 61 fields · synced May 22, 2026