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Skinuvita Phototherapy Solution

EUDAMED

Class IIa (EU MDR)

Ref PTMS

by Skinuvita GmbH

Identity

Trade Name
Skinuvita Phototherapy Solution EUDAMED
Device Name
Skinuvita Phototherapy Solution EUDAMED
Model / Reference
PTMS EUDAMED

Identifiers

Primary DI / UDI-DI
04262439760078 EUDAMED
Basic UDI-DI
426243976PTMSHH EUDAMED
Direct Marketing DI
04262439760078 EUDAMED
EMDN Code
V92 MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Special Device Type
Software 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

Skinuvita Phototherapy Solution by Skinuvita 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
Skinuvita GmbH
EUDAMED SRN
DE-MF-000038977

Sources (1)

  • EUDAMED b7a55c8a-94f0-4176-85f5-0e7ff863b8cd 61 fields · synced Sep 18, 2026