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Revolution ACTs

by Wipro GE Healthcare Private Limited

Ref Revolution ACTsModel Yes

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00198953187890 Basic UDI-DI 00198953187890UDI-DIDate9 Sep 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  • Withdrawn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

Model / Reference
Yes, Revolution ACTs
Primary DI / UDI-DI
00198953187890
Basic UDI-DI
B-00198953187890
EMDN Code
Z11030602 Computed tomographs - exceeding 2 layers but less than 16 layers
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IN-MF-000016091
Authorised representative
GE Medical Systems SCS FR-AR-000000344

Other devices from Wipro GE Healthcare Private Ltd

See all devices from Wipro GE Healthcare Private Ltd →

Properties

  • Measuring Function

Other properties (10)

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