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InfoSmart Web High Flow

by Fisher & Paykel Healthcare Limited 7 variants

Ref 622991

InfoSmart Web High Flow (622991) is a Class IIb device made by Fisher & Paykel Healthcare Limited, registered in EUDAMED on 2 Oct 2026 (Basic UDI-DI 94200124INFOSMARTWEB02X2), active as of 8 Nov 2026.

Active European Union

CE MDR

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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number94200124INFOSMARTWEB02X2 Basic UDI-DI 09420012478849UDI-DIDate2 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
622991
Primary DI / UDI-DI
09420012478849
Basic UDI-DI
94200124INFOSMARTWEB02X2
EMDN code
Z1203019082 Various instruments for anaesthesia and pulmonary ventilation support - software accessories
Device class
Class IIb
Special device type
Software
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
NZ-MF-000002556
Authorised representative
FISHER & PAYKEL HEALTHCARE SAS FR-AR-000000294

Similar devices in this category

Other devices filed under VARIOUS INSTRUMENTS FOR ANAESTHESIA AND PULMONARY VENTILATION SUPPORT.

Other devices from Fisher & Paykel Healthcare Limited

See all devices from Fisher & Paykel Healthcare Limited →

Properties

Other properties (14, all answered No)