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iClean Viral Transport System (VTM-RT)

by Huachenyang (Shenzhen) Technology Co., Ltd. 17 variants

Ref CY-A-F005-20Model CY-A-F005-00, CY-A-F005-10, CY-A-F005-20, CY-A-F005-30, CY-B-F005-00, CY-B-F005-10, CY-B-F005-20, CY-B-F005-25, CY-B-F005-30, CY-F003-40,CY-F005-20, CY-F003-40(NGS)

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

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/IVDR Number697448899CY-F0/0/5/2/8V7Z Basic UDI-DI 06974488991584UDI-DIDate8 Apr 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Model / Reference
CY-A-F005-00, CY-A-F005-10, CY-A-F005-20, CY-A-F005-30, CY-B-F005-00, CY-B-F005-10, CY-B-F005-20, CY-B-F005-25, CY-B-F005-30, CY-F003-40, CY-F005-20, CY-F003-40(NGS)
Primary DI / UDI-DI
06974488991584
Basic UDI-DI
697448899CY-F0/0/5/2/8V7Z
EMDN Code
A1102 Sample collection swabs with transport medium
Device Class
Class A
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000020236
Authorised representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Other devices from Huachenyang (Shenzhen) Technology Co., Ltd

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Properties

  • Reagent

Other properties (10)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No