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Tempdrop Fertility Monitor

by Tempdrop LTD

Ref TD-REF-1

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 linked in EUDAMED

A group certificate may exist

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 Number08600011164TD1HJ Basic UDI-DI 00860001116472UDI-DIDate3 Sep 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Tempdrop Fertility Monitor
Model / Reference
TD-REF-1
Primary DI / UDI-DI
00860001116472
Basic UDI-DI
08600011164TD1HJ
Direct Marketing DI
00860001116472
EMDN Code
V03010199 Thermometers - other
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
IL-MF-000029159
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

From the manufacturer

Manufacturer's product page: here

Other devices from Tempdrop 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