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SurgiCube

by Toul Meditech AB 2 variants

Ref SC220

SurgiCube (SC220) is a Class I device made by Toul Meditech AB, registered in EUDAMED on 26 May 2026 (Basic UDI-DI 87202997481SCI95), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number87202997481SCI95 Basic UDI-DI 08720299748125UDI-DIDate26 May 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  • Withdrawn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
SC220
Primary DI / UDI-DI
08720299748125
Basic UDI-DI
87202997481SCI95
EMDN code
V0899 Medical support equipment - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
SE-MF-000005195

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Properties

Other properties (14, all answered No)