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CORELab

by Medimaps Group SA

Ref CORELABModel Software Accessory for medical image communication

CORELab is a Class I device made by medimaps group SA, registered in EUDAMED on 19 Jun 2026 (Basic UDI-DI ++B214CORELABQJ), active as of 24 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++B214CORELABQJ Basic UDI-DI +B214CORELABV100UDI-DIDate19 Jun 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  • Withdrawn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

Model / reference
Software Accessory for medical image communication, CORELAB
Primary DI / UDI-DI
+B214CORELABV100
Basic UDI-DI
++B214CORELABQJ
Direct marketing DI
+B214CORELABV100
EMDN code
Z11900182 Bone densitometry systems - software accessories
Device class
Class I
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
CH-MF-000039146
Authorised representative
Med-Imaps SASU FR-AR-000038706

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Other devices filed under BONE DENSITOMETRY SYSTEMS.

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Properties

Other properties (14, all answered No)