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TECO® Human Intact Proinsulin ELISA

by TECOmedical AG Switzerland EUDAMED

Ref TE1012

EMDN W0102060107

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-07640146270016 Basic UDI-DIDate27 Dec 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/IVDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
TECO® Human Intact Proinsulin ELISA
Model / Reference
TE1012
Primary DI / UDI-DI
07640146270016
Basic UDI-DI
B-07640146270016
EMDN Code
W0102060107 Proinsulin
Device Class
Class IVD General
Market of Registration
France

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 1b87d6a0-fe94-446f-be6b-e6ad782b8d3f 61 fields · synced 22 Oct 2026