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Upper Arm Blood Pressure Monitor

by Famidoc Technology Co., Ltd.

Ref FDBP-A13

Active European Union

CE MDR

Valid until

10 Jul 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SGS Belgium NV

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberCN23/00003635 Date30 Sep 2024IssuedStatusActive expires 10 Jul 2028

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • CN23/00003635 Active Amended

    Quality management system EU MDR

    Certifier
    SGS Belgium NV 1639
    Issued
    30 Sep 2024
    Expires
    10 Jul 2028
    Reason
    Mnf ar change

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
FDBP-A13
Primary DI / UDI-DI
06970389631598, 06970389632649
Basic UDI-DI
697038963FDBPN8
EMDN Code
Z1203020302 Non–invasive blood pressure monitoring instruments
Device Class
Class IIa
EU market of registration
Germany
Denmark

Manufacturer details

EUDAMED SRN
CN-MF-000016603
Authorised representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Other devices from Famidoc Technology Company Limited

See all devices from Famidoc Technology Company Limited →

Properties

  • Measuring Function

Other properties (12)

  • 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
  • Incorporates Medicinal Product: No