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Anesthesia Machine

by Atlantamed Ltd. EUDAMED

Active European Union

Ref 135100081Model Diora

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-5065016237DioraAE6G Basic UDI-DIDate15 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Specification

EUDAMED

Device Name
Anesthesia Machine
Model / Reference
Diora, 135100081
Primary DI / UDI-DI
D-5065016237DioraAE6G
Basic UDI-DI
B-5065016237DioraAE6G
EMDN Code
R9080 Respiratory and anesthesia devices - accessories not included in other classes
Device Class
Class IIb
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
UK-MF-000038727
Authorised representative
Casus Europe B.V. NL-AR-000037688

Other devices from Atlantamed Ltd.

Properties

  • Administering Medicine
  • Measuring Function

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Incorporates Medicinal Product: No