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SeQuent®

by B. Braun Melsungen AG 49 variants

Ref 5023424

Active European Union

CE MDR

Valid until

6 Sep 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV SÜD Product Service GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

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

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • G70 012974 0637 Active Amended

    Technical documentation EU MDR

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

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
SeQuent Please GROUP
Model / Reference
5023424
Primary DI / UDI-DI
04046955925018
Basic UDI-DI
40392390000013492K
EMDN Code
C010401020199 Ptca dilatation catheters - other
Device Class
Class III
EU 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

  • 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