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microFET2 device with MicroFET software

by Hoggan Scientific

Part of a family of 16 devices: see the family page

Ref 5021-C

microFET2 device with MicroFET software (5021-C) is a medical device (EU MDR Class I) made by Hoggan Scientific, LLC, registered in EUDAMED on 31 Aug 2026 (Basic UDI-DI 850002429microFETHP), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number850002429microFETHP Basic UDI-DI 00850002429015UDI-DIDate31 Aug 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
microFET
Model / reference
5021-C
Primary DI / UDI-DI
00850002429015
Basic UDI-DI
850002429microFETHP
EMDN code
Z12062680, Z12062692
Device class
Class I
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000038068
Authorised representative
Emergo Europe B.V. NL-AR-000000116

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Properties

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