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Hand Rail

by Famica International Co. Ltd.

Ref AH20 (AAH020-XXX、SAH020-XXX)Model AH20(AAH020-XXX、SAH020-XXX)

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number471988023AHM0039B Basic UDI-DI 04719880230105UDI-DIDate27 May 2025RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Hand Rail
Model / Reference
AH20(AAH020-XXX、SAH020-XXX), AH20 (AAH020-XXX、SAH020-XXX)
Primary DI / UDI-DI
04719880230105
Basic UDI-DI
471988023AHM0039B
EMDN Code
Y181803 Handrails
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
TW-MF-000034084
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Famica International Co. 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