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ECO Maxi Angled Coil Paper HME

by GVS Filter Technology UK Limited 2 variants

Ref 4333/770BRSA001/0001

Active European Union

CE MDR

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506012095Cat175 Basic UDI-DI 05060511622134UDI-DIDate29 May 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Humidification Systems
Model / Reference
4333/770BRSA001/0001
Primary DI / UDI-DI
05060511622134
Basic UDI-DI
506012095Cat175
EMDN Code
R040201 Tracheostomy humidifiers
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
UK-MF-000045036
Authorised representative
GVS S.p.A. IT-AR-000028148

Other devices from GVS Filter Technology UK Ltd

See all devices from GVS Filter Technology UK Ltd →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No