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SeQuent®

by B. Braun Melsungen AG 49 variants

Ref 5023406

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  • Withdrawn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

EU market availability

Made available in 27 countries, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Austria since 12 May 2026
  • Belgium since 12 May 2026
  • Bulgaria since 12 May 2026
  • Croatia since 12 May 2026
  • Cyprus since 12 May 2026
  • Czechia since 12 May 2026
  • Denmark since 12 May 2026
  • Estonia since 12 May 2026
  • Finland since 12 May 2026
  • France since 12 May 2026
  • Germany since 12 May 2026
  • Greece since 12 May 2026
  • Hungary since 12 May 2026
  • Ireland since 12 May 2026
  • Italy since 12 May 2026
  • Latvia since 12 May 2026
  • Lithuania since 12 May 2026
  • Luxembourg since 12 May 2026
  • Malta since 12 May 2026
  • Netherlands since 12 May 2026
  • Poland since 12 May 2026
  • Portugal since 12 May 2026
  • Romania since 12 May 2026
  • Slovakia since 12 May 2026
  • Slovenia since 12 May 2026
  • Spain since 12 May 2026
  • Sweden since 12 May 2026

Last checked 24 Oct 2026.

Specification

EUDAMED

Device Name
SeQuent Please GROUP
Model / Reference
5023406
Primary DI / UDI-DI
04046955924684
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