Skip to content

Electret Snore Sensor for Medatec (150 cm) - Key Connector

by S.L.P. Ltd.

Ref MMICA-KYLModel 12XX series

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7290012186SN001TY Basic UDI-DI 07290016716429UDI-DIDate27 Oct 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Snore Sensors
Model / Reference
12XX series, MMICA-KYL
Primary DI / UDI-DI
07290016716429
Basic UDI-DI
7290012186SN001TY
EMDN Code
Z1399 Non-specific consumables for diagnostic instruments - other
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IL-MF-000016600
Authorised representative
Arazy Group GmbH DE-AR-000007685

Other devices from S.L.P. Ltd.

See all devices from S.L.P. Ltd. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No