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SeQuent®

by B. Braun Melsungen AG Germany EUDAMED

Ref 5023403

EMDN C010401020199

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberG70 012974 0637 Date16 Jul 2026IssuedStatusActive expires 6 Sep 2028

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • G70 012974 0637 Amended

    Technical documentation EU MDR

    Notified body
    TÜV SÜD Product Service GmbH 0123
    Issued
    16 Jul 2026
    Expires
    6 Sep 2028
    Reason
    Other

Specification

EUDAMED · synced 22 Oct 2026

Device Name
SeQuent Please GROUP
Model / Reference
5023403
Primary DI / UDI-DI
04046955924660
Basic UDI-DI
40392390000013492K
EMDN Code
C010401020199 Ptca dilatation catheters - other
Device Class
Class III
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000000201

Other devices from B. Braun Melsungen AG

See all devices from B. Braun Melsungen AG →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Incorporates Medicinal Product
Other properties (11)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No

Sources (1)

  • EUDAMED 653f6319-2658-416d-9ba5-36a32a1e505d 61 fields · synced 22 Oct 2026