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swiftPAC Coil, 3 cm

by Penumbra, Inc. EUDAMED

Active European Union

Ref 400SWPC03Model Embolization Coils

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberMDR 739883 Date22 Jun 2026IssuedStatusActive expires 28 Mar 2028

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 739883 Active Supplemented

    Technical documentation EU MDR

    Notified body
    BSI Group The Netherlands B.V. 2797
    Issued
    22 Jun 2026
    Expires
    28 Mar 2028
    Reason
    Other

Specification

EUDAMED

Device Name
Penumbra Embolization Coil System
Model / Reference
Embolization Coils, 400SWPC03
Primary DI / UDI-DI
00810169721452
Basic UDI-DI
081454801PCOEU
EMDN Code
C010402020301 Embolisation coils
Device Class
Class III
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000008514
Authorised representative
Penumbra Europe GmbH DE-AR-000004997

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Properties

  • Sterile
  • Implantable
  • CMR Substance

Other properties (10)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No