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Oropharyngeal Airway

by Xiamen Compower Medical Tech. Co., Ltd. 23 variants

Ref 09851Model Z40、Z50、Z60、Z70、Z80、Z90、Z100、Z110、Z120、Z40～Z110、Z40～Z120

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number694643043130801N2 Basic UDI-DI 06946430427441UDI-DIDate15 Mar 2024RegisteredStatusActive

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  • Withdrawn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

Model / Reference
Z40、Z50、Z60、Z70、Z80、Z90、Z100、Z110、Z120、Z40～Z110、Z40～Z120, 09851
Primary DI / UDI-DI
06946430427441
Basic UDI-DI
694643043130801N2
EMDN Code
R010102 Guedel airway tubes
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000011703
Authorised representative
Sungo Cert GmbH DE-AR-000010869

Other devices from Xiamen Compower Medical Tech. Co., Ltd.

See all devices from Xiamen Compower Medical Tech. Co., 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