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OOM101 Max

by Honeywell Healthcare Solutions GmbH

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

Ref E1002659

OOM101 Max (E1002659) is a Class IIa device made by Honeywell Healthcare Solutions GmbH, registered in EUDAMED on 21 Sep 2026 (Basic UDI-DI 4036616OOMCK), active as of 22 Oct 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4036616OOMCK Basic UDI-DI 04036616011334UDI-DIDate21 Sep 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Sauersoffsensor OOM-Familie
Model / reference
E1002659
Primary DI / UDI-DI
04036616011334
Basic UDI-DI
4036616OOMCK
EMDN code
R9080 Respiratory and anesthesia devices - accessories not included in other classes
Device class
Class IIa
EU registration type
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)