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Imoove-300

by Allcare Innovations

Ref IMOOVE-300

Imoove-300 is a Class I device made by Allcare Innovations, registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI 3770028850IMM8C), active as of 7 Nov 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3770028850IMM8C Basic UDI-DI Date27 Oct 2026RegisteredStatusActive

Official records

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device name
Imoove
Model / reference
IMOOVE-300
Primary DI / UDI-DI
03770028850020, 03770028850037
Basic UDI-DI
3770028850IMM8C
Direct marketing DI
03770028850020
03770028850037
EMDN code
Z120602 Physiotherapy equipment
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany
Bulgaria

Manufacturer details

EUDAMED SRN
FR-MF-000056472

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Properties

Other properties (14, all answered No)