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Demand Valve

by BNOS MediTECH Ltd 24 variants

Ref 900-0030-00Model Analgesic Demand Valve (2M Hose0 DIN Fitting

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDD, withdrawn

Ended

Withdrawn

Date not published (CE MDD)

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05052270000476 Basic UDI-DI 05052270000476UDI-DIDate1 Jul 2026RegisteredStatusWithdrawn No longer placed on the EU market

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.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Withdrawn

Specification

EUDAMED

Model / Reference
Analgesic Demand Valve (2M Hose0 DIN Fitting, 900-0030-00
Primary DI / UDI-DI
05052270000476
Basic UDI-DI
B-05052270000476
EMDN Code
R028001 Respiratory circuits valves
Device Class
Class IIa

Manufacturer details

EUDAMED SRN
GB-MF-000008883
Authorised representative
Medical Device Management Ltd IE-AR-000002496

Other devices from B.N.O.S. Meditech Limited

See all devices from B.N.O.S. Meditech Limited →

Properties

  • Administering Medicine

Other properties (10)

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