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Pegasos

by CGI Suomi Oy EUDAMED

Withdrawn No longer placed on the EU market

Ref Pegasos v9.2

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-Pegasos9.23Y Basic UDI-DIDate12 Dec 2025RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Withdrawn

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Pegasos
Model / Reference
Pegasos v9.2
Primary DI / UDI-DI
D-Pegasos9.23Y
Basic UDI-DI
B-Pegasos9.23Y
EMDN Code
V92 Medical device software - not included in other classes
Device Class
Class I
Special Device Type
-1192

Manufacturer details

EUDAMED SRN
FI-MF-000012661

Other devices from CGI Suomi Oy

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