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Sanico

by Xuzhou Yongkang Electronic Science Technology Co., Ltd.

Part of a family of 18 devices: see the family page

Ref YK-81C

Sanico (YK-81C) is a Class IIa device made by Xuzhou Yongkang Electronic Science Technology Co., Ltd, registered in EUDAMED on 19 Dec 2024 (Basic UDI-DI 69217452FPO2V), active as of 24 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69217452FPO2V Basic UDI-DI 06921745206127UDI-DIDate19 Dec 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Fingertip Pulse Oximeter
Model / reference
YK-81C
Primary DI / UDI-DI
06921745206127
Basic UDI-DI
69217452FPO2V
Direct marketing DI
06921745206127
EMDN code
Z1203020408 Pulse oximeters
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
CN-MF-000018890
Authorised representative
Prolinx GmbH DE-AR-000005129

Similar devices in this category

Other devices filed under PULSE OXIMETERS.

Other devices from Xuzhou Yongkang Electronic Science Technology Co., Ltd

See all devices from Xuzhou Yongkang Electronic Science Technology Co., Ltd →

Properties

  • Measuring function
Other properties (13, all answered No)