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Saalux

EUDAMED

Class IIa (EU MDR)

Ref 07-02-000-03

by Saalmann medical GmbH & Co. KG

Identity

Trade Name
Saalux EUDAMED
Device Name
Saalux UV Kamm (UVB 311nm) DE EUDAMED
Model / Reference
07-02-000-03 EUDAMED

Identifiers

Primary DI / UDI-DI
04260587511030 EUDAMED
Basic UDI-DI
426058751SAALUXDK EUDAMED
Direct Marketing DI
04260587511030 EUDAMED
EMDN Code
Z12040202 PHOTOTHERAPY EQUIPMENT EUDAMED

Classification

Device Class
Class IIa 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

Saalux by Saalmann medical GmbH & Co. KG — 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

EUDAMED SRN
DE-MF-000010552

Sources (1)

  • EUDAMED d351971f-3259-4fed-9917-f57f31ee99ef 61 fields · synced Oct 6, 2026