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Flexible

by Microlife Corporation

Ref FlexibleModel MT1P21

Flexible is a Class IIa device made by Microlife Corporation, registered in EUDAMED on 19 Oct 2026 (Basic UDI-DI B-M199051P211003024), active as of 7 Nov 2026.

Active European Union

CE MDD

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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-M199051P211003024 Basic UDI-DI D-M199051P211003024UDI-DIDate19 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Flexible
Model / reference
MT1P21, Flexible
Primary DI / UDI-DI
D-M199051P211003024
Basic UDI-DI
B-M199051P211003024
EMDN code
V0301010201 Contact digital thermometers (including probes)
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
TW-MF-000010688
Authorised representative
Microlife UAB LT-AR-000011673

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Other devices filed under CONTACT DIGITAL THERMOMETERS (INCLUDING PROBES).

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Properties

  • Measuring function
Other properties (11, all answered No)