Skip to content

Suru

by Suru International Pvt Ltd 82 variants

Part of a family of 8 devices: see the family page

Ref 3023.2Model 3023

Suru (3023.2) is a Class IIa device made by Suru International Pvt Ltd, registered in EUDAMED on 16 Jun 2026 (Basic UDI-DI 89021413023PU), active as of 7 Nov 2026.

Active European Union

CE MDR 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number89021413023PU Basic UDI-DI 08902141101030UDI-DIDate16 Jun 2026RegisteredStatusActive
European UnionCE/MDR Number89021413023PU Basic UDI-DI 08902141101030UDI-DIDate16 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD, CE/MDR Active

Specification

EUDAMED

Device name
Guedel Airways (Oro-Pharyngeal Airways)
Model / reference
3023, 3023.2
Primary DI / UDI-DI
08902141101030
Basic UDI-DI
89021413023PU, B-08902141101030
EMDN code
R010102 Guedel airway tubes
Device class
Class IIa
System or procedure pack
System which is a device in itself
EU registration type
Standard device
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IN-MF-000023736
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Similar devices in this category

Other devices filed under GUEDEL AIRWAY TUBES.

Other devices from Suru International Pvt Ltd

See all devices from Suru International Pvt Ltd →

Properties

  • Supplied sterile
Other properties (13, all answered No)