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Dermatoscope

EUDAMED

Class I (EU MDR)

Ref FMO-001-1700-2095

by SG Manufacturers

Identity

Trade Name
DERMATOSCOPE EUDAMED
Device Name
DERMATOSCOPE EUDAMED
Model / Reference
FMO-001-1700-2095 EUDAMED

Identifiers

Primary DI / UDI-DI
08964004012655 EUDAMED
Basic UDI-DI
8964003248DM045R EUDAMED
EMDN Code
Z12040108 DERMATOSCOPES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Dermatoscope by SG Manufacturers — 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
SG Manufacturers
EUDAMED SRN
PK-MF-000007106
Authorised Representative
International Business Compendious of Sweden SE-AR-000001625

Sources (1)

  • EUDAMED 441903b5-e9f3-4ae8-8d5d-dd443a8ace96 61 fields · synced Jul 24, 2026