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SOMNOtouch™ RESP

EUDAMED

Class IIa (EU MDR)

Ref TOR050Model SOMNOtouch

by SOMNOmedics AG

Identity

Trade Name
SOMNOtouch™ RESP EUDAMED
Model / Reference
SOMNOtouch EUDAMED
TOR050 EUDAMED

Identifiers

Primary DI / UDI-DI
04250413404384 EUDAMED
Basic UDI-DI
42504134PSGSC EUDAMED
EMDN Code
Z12100501 POLYSOMNOGRAPHS 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

SOMNOtouch™ RESP by SOMNOmedics AG — 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
SOMNOmedics AG
EUDAMED SRN
DE-MF-000006921

Sources (1)

  • EUDAMED 7ad5cb62-1b9f-4c5f-a62c-bf2948dc8df2 61 fields · synced Jun 19, 2026