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ST2308

by Shenzhen SINO-K Medical Technology Co., Ltd.

Ref 07-10-00Model ST2308

Active European Union

CE MDD

Valid until

Not listed

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

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/MDD NumberB-06972820961257 Basic UDI-DI 06972820961257UDI-DIDate11 Oct 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Temperature Probe
Model / Reference
ST2308, 07-10-00
Primary DI / UDI-DI
06972820961257
Basic UDI-DI
B-06972820961257
EMDN Code
V03010201 Temperature monitoring cutaneous probes
Device Class
Class IIa
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
CN-MF-000021157
Authorised representative
Prolinx GmbH DE-AR-000005129

Related devices

Category: General-purpose patient temperature probe, reusable

Other devices from Shenzhen SINO-K Medical Technology Co., Ltd

See all devices from Shenzhen SINO-K Medical Technology Co., Ltd →

Properties

  • Reusable
  • Measuring Function

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No