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Robotic Ultrasound System (Doctor-end)MGIUS-R3D

by Wuhan MGI Tech Co., Ltd.

Ref 900-000219-00

Active European Union

CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06974318130749 Basic UDI-DI 06974318130749UDI-DIDate19 Mar 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Robotic Ultrasound System
Model / Reference
900-000219-00
Primary DI / UDI-DI
06974318130749
Basic UDI-DI
B-06974318130749
EMDN Code
Z11040199 Ultrasound scanners - other
Device Class
Class IIa
EU market of registration
Latvia

Manufacturer details

EUDAMED SRN
CN-MF-000018732
Authorised representative
Latvia MGI Tech SIA LV-AR-000017789

Other devices from Wuhan MGI Tech Co., Ltd.

See all devices from Wuhan MGI Tech Co., Ltd. →

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No