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Hose Assembly

by BNOS MediTECH Ltd 31 variants

Ref 131-0467-00Model O2 Hose Assembly,4M, Afnor Probe to Afnor Probe (Thin Hose)

Active European Union

CE MDD

Valid until

Not listed

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

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-05052270602755 Basic UDI-DI 05052270602755UDI-DIDate23 Sep 2026RegisteredStatusActive

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  • Withdrawn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 Active

Specification

EUDAMED

Model / Reference
O2 Hose Assembly, 4M, Afnor Probe to Afnor Probe (Thin Hose), 131-0467-00
Primary DI / UDI-DI
05052270602755
Basic UDI-DI
B-05052270602755
EMDN Code
R9080 Respiratory and anesthesia devices - accessories not included in other classes
Device Class
Class IIa
EU market of registration
France

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