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MavieMe Home Blood Test Kit

by MavieMe GmbH 3 variants

Ref MMB

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number5065012100MMBVV Basic UDI-DI 05065012100105UDI-DIDate30 Jun 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name
MavieMe Home Blood Test Kit (Gold and Lavender Tubes)
Model / Reference
MMB
Primary DI / UDI-DI
05065012100105
Basic UDI-DI
5065012100MMBVV
Direct Marketing DI
05065012100105
EMDN Code
W050101010201, W0501010201
Device Class
Class A
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
AT-MF-000046815

Other devices from MavieMe GmbH

Properties

  • Self Testing
  • Near-Patient Testing
  • Professional Testing

Other properties (8)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No