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TECO® Human Leptin ELISA kit

by TECOmedical AG Switzerland EUDAMED

Ref TE1015 EMDN W0102069014

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-07640146270030 Basic UDI-DIDate27 Dec 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/IVDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Device Name
TECO® Human Leptin ELISA kit
Model / Reference
TE1015
Primary DI / UDI-DI
07640146270030
Basic UDI-DI
B-07640146270030
EMDN Code
W0102069014 Leptin
Device Class
Class IVD General
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000030341
Authorised representative
EUROBIO SCIENTIFIC FR-AR-000023178

Other devices from TECOmedical AG

See all devices from TECOmedical AG →

Properties & raw data

Show properties, registry sources and raw records
  • Professional Testing
Other properties (9)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No

Sources (1)

  • EUDAMED 4b1106b8-0763-49cb-a805-c029d0129f59 61 fields · synced 25 Oct 2026