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SIGKNOW EZYPRO ECG Patch UG02-P

by Sigknow Biomedical Co., Ltd. 2 variants

Ref UG02-PModel UG02-P, UG02-PL, UG03-P1, UG03-P3S, UG03-P3C

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0471987501PATCH6G Basic UDI-DI Date5 Nov 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  • Withdrawn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
SIGKNOW EZYPRO ECG Patch
Model / Reference
UG02-P, UG02-PL, UG03-P1, UG03-P3S, UG03-P3C
Primary DI / UDI-DI
04719875010514, 04719875010194
Basic UDI-DI
0471987501PATCH6G
EMDN Code
C020501 ECG electrodes
Device Class
Class I
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
TW-MF-000026397
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from Sigknow Biomedical Co., Ltd.

See all devices from Sigknow Biomedical 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