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Guedel Airways for Single Use

by Shaoxing Undis Medical Technology Co., Ltd 5 variants

Ref 12 specification 12

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 linked in EUDAMED

A group certificate may exist

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 Number697053133gasuX8 Basic UDI-DI 16970531333346UDI-DIDate20 Apr 2024RegisteredStatusActive EUDAMED: not on the EU market

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
No
Model / Reference
12 specification 12
Primary DI / UDI-DI
16970531333346
Basic UDI-DI
697053133gasuX8
Direct Marketing DI
16970531333346
EMDN Code
R010102 Guedel airway tubes
Device Class
Class IIa

Manufacturer details

EUDAMED SRN
CN-MF-000002187
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Shaoxing Undis Medical Technology Co., Ltd

See all devices from Shaoxing Undis Medical Technology Co., Ltd →

Properties

  • Sterile

Other properties (12)

  • 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