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INQOx

by Honeywell Healthcare Solutions GmbH

Ref AA844-210

INQOx (AA844-210) is a Class IIa device made by Honeywell Healthcare Solutions GmbH, registered in EUDAMED on 24 Jul 2026 (Basic UDI-DI B-04036616013703), active as of 24 Oct 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberB-04036616013703 Basic UDI-DI 04036616013703UDI-DIDate24 Jul 2026RegisteredStatusActive
European UnionCE/MDD NumberB-04036616013703 Basic UDI-DI 04036616013703UDI-DIDate24 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR, CE/MDD Active

Specification

EUDAMED

Device name
INQOx
Model / reference
AA844-210
Primary DI / UDI-DI
04036616013703
Basic UDI-DI
B-04036616013703, 4036616INQOXVD
EMDN code
R9080 Respiratory and anesthesia devices - accessories not included in other classes
Device class
Class IIa
EU registration type
Legacy device (under a directive)
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000004924

Similar devices in this category

Other devices filed under RESPIRATORY AND ANESTHESIA DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES.

Other devices from Honeywell Healthcare Solutions GmbH

See all devices from Honeywell Healthcare Solutions GmbH →

Properties

Other properties (14, all answered No)