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Electret Snore Sensor for P Series

EUDAMED

Class I (EU MDR)

Ref 1205Model 12XX series

by S.L.P. Ltd.

Identity

Trade Name
Electret Snore Sensor for P Series EUDAMED
Device Name
Snore Sensors EUDAMED
Model / Reference
12XX series EUDAMED
1205 EUDAMED

Identifiers

Primary DI / UDI-DI
07290008986748 EUDAMED
Basic UDI-DI
7290012186SN001TY EUDAMED
EMDN Code
Z1399 NON-SPECIFIC CONSUMABLES FOR DIAGNOSTIC INSTRUMENTS - OTHER 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

Electret Snore Sensor for P Series by S.L.P. Ltd. — 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
S.L.P. Ltd.
EUDAMED SRN
IL-MF-000016600
Authorised Representative
Arazy Group GmbH DE-AR-000007685

Sources (1)

  • EUDAMED ab86928e-2dd6-433b-94cd-909427df739a 61 fields · synced Aug 2, 2026