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Eu-941

by Ito Co., Ltd.

Ref EU-941

Eu-941 is a Class IIa device made by Ito Co., Ltd., registered in EUDAMED on 10 Mar 2026 (Basic UDI-DI B-04983087010772), active as of 22 Oct 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04983087010772 Basic UDI-DI 04983087010772UDI-DIDate10 Mar 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
EU-941
Primary DI / UDI-DI
04983087010772
Basic UDI-DI
B-04983087010772
EMDN code
Z120601, Z120610
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
JP-MF-000021681
Authorised representative
MDSS GmbH DE-AR-000005430

Similar devices in this category

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See all devices from Ito Co., Ltd. →

Properties

Other properties (12, all answered No)