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Electronic Blood Pressure Monitor

by Zhongshan Jinli Electronic Weighing Equipment Co., Ltd. 3 variants

Ref AP8030Model AP8010, AP8020, AP8030

Active European Union

CE MDR

Valid until

25 Nov 2030

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberCN25/00007955 Date5 Feb 2026IssuedStatusActive expires 25 Nov 2030

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • CN25/00007955 Active

    Quality management system EU MDR

    Certifier
    SGS Belgium NV 1639
    Issued
    5 Feb 2026
    Expires
    25 Nov 2030

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
AP8010, AP8020, AP8030
Primary DI / UDI-DI
06973337428011
Basic UDI-DI
697333742801KU
Direct Marketing DI
06973337428011
EMDN Code
Z1203020302 Non–invasive blood pressure monitoring instruments
Device Class
Class IIa
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
CN-MF-000021308
Authorised representative
Wellkang Ltd XI-AR-000001836

Other devices from Zhongshan Jinli Electronic Weighing Equipment Co., Ltd.

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