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Paradym Rf Dr 9550

by MicroPort CRM S.r.l. Italy EUDAMED

Ref TDF025CModel PARADYM RF DR 9550 EMDN J01050201

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/AIMDD NumberB-08031527013923 Basic UDI-DIDate18 Sep 2026RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/AIMDD Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
PARADYM - Implantable Cardioverter Defibrillators
Model / Reference
PARADYM RF DR 9550, TDF025C
Primary DI / UDI-DI
08031527013923
Basic UDI-DI
B-08031527013923
EMDN Code
J01050201 Implantable dual chamber defibrillators, with sensors
Device Class
Class AIMDD

Manufacturer details

EUDAMED SRN
IT-MF-000029013

Other devices from MicroPort CRM S.r.l.

See all devices from MicroPort CRM S.r.l. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
Other properties (9)
  • 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

Sources (1)

  • EUDAMED 08031527013923|B-08031527013923 61 fields · synced 24 Oct 2026