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Myosa K

by Myofunctional Research Co. EUDAMED

Active European Union

Ref 705031, 705020

Overview

Myosa K is a medical device designed to provide effective anti-snoring solutions for individuals who suffer from this condition. It utilizes advanced technology and innovative design to alleviate symptoms and improve sleep quality.

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number9330944A0000002MP Basic UDI-DIDate25 Oct 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Anti-Snoring devices
Model / Reference
705031, 705020
Primary DI / UDI-DI
19330944001220, 19330944002272
Basic UDI-DI
9330944A0000002MP
EMDN Code
Q03010299 Antisnoring and obstructive sleep apnoea devices - other
Device Class
Class I
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
AU-MF-000011059
Authorised representative
Myofunctional Research Europe B.V. NL-AR-000003918

Other devices from Myofunctional Research Co.

See all devices from Myofunctional Research Co. →

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