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Fabian Connecting Limb – 56cm

by Viomedex Ltd

Ref IHC615/10

Active European Union

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05060206921108 Basic UDI-DI 05060206921108UDI-DIDate22 Oct 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  • Withdrawn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

Device name
Neontal Breathing Circuits
Model / reference
IHC615/10
Primary DI / UDI-DI
05060206921108
Basic UDI-DI
B-05060206921108
EMDN code
R02010401 Cpap circuits
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Estonia

Manufacturer details

EUDAMED SRN
GB-MF-000004399
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Viomedex Ltd

See all devices from Viomedex Ltd →

Properties

  • Administering medicine

Other properties (11)

  • Supplied sterile: No
  • Sterilise before use: No
  • Implantable: No
  • Reusable: No
  • Contains latex: No
  • Reprocessed single-use device: No
  • Incorporates a substance derived from human blood or plasma: No
  • Contains human tissues or cells: No
  • Contains animal tissues or cells: No
  • Measuring function: No
  • Incorporates a medicinal substance: No