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Guedal Airway

by Disposafe Health & Lifecare Limited 13 variants

Ref GUA3Model GUA35

Guedal Airway (GUA3) is a Class I device made by Disposafe Health & Lifecare Limited, registered in EUDAMED on 14 Sep 2026 (Basic UDI-DI B-GUA3), active as of 23 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-GUA3 Basic UDI-DI Date14 Sep 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Guedel(oropharyngeal) airway, Size 3
Guedel(oropharyngeal) airway, Size 3.5
Model / reference
GUA3, GUA35
Primary DI / UDI-DI
GUA3, GUA35
Basic UDI-DI
B-GUA3, B-GUA35
EMDN code
R010102 Guedel airway tubes
Device class
Class I
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
IN-MF-000020265
Authorised representative
AR Experts B.V. NL-AR-000023989

Similar devices in this category

Other devices filed under GUEDEL AIRWAY TUBES.

Other devices from Disposafe Health & Lifecare Limited

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Properties

  • Supplied sterile
Other properties (11, all answered No)