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SELUTION SLR™ 018 PTA Balloon Catheter

by M.A. Med Alliance SA 56 variants

Ref SE18-060150

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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/MDD NumberB-07640278880350 Basic UDI-DI 07640278880350UDI-DIDate16 Jul 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

NorwayIcelandSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaLiechtensteinAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyTürkiyeCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

EU market availability

Made available in 32 countries, as listed in EUDAMED:

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

  • Austria since 27 Dec 2021
  • Belgium
  • Bulgaria since 21 Mar 2022
  • Croatia since 8 Dec 2021
  • Cyprus since 2 May 2022
  • Czechia since 1 Jun 2025
  • Denmark
  • Estonia
  • Finland since 17 Sep 2020
  • France since 1 Feb 2024
  • Germany since 10 Aug 2020
  • Greece since 6 Oct 2020
  • Hungary since 1 Mar 2024
  • Iceland
  • Ireland since 18 May 2021
  • Italy since 14 Oct 2020
  • Latvia since 1 Mar 2024
  • Liechtenstein
  • Lithuania since 28 Sep 2022
  • Luxembourg
  • Malta
  • Netherlands since 30 Dec 2020
  • Northern Ireland
  • Norway
  • Poland since 30 Jul 2021
  • Portugal since 1 Mar 2023
  • Romania since 16 Feb 2021
  • Slovakia since 30 Dec 2020
  • Slovenia since 29 Aug 2022
  • Spain since 7 Apr 2022
  • Sweden
  • Türkiye since 30 Dec 2022

Last checked 23 Oct 2026.

Specification

EUDAMED

Device Name
SELUTION SLR™ PTA Balloon Catheter
Model / Reference
SE18-060150
Primary DI / UDI-DI
07640278880350
Basic UDI-DI
B-07640278880350
EMDN Code
C010402020199 PTA dilatation catheters - other
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000025422
Authorised representative
MedAlliance Germany GmbH DE-AR-000023728

Other devices from M.A. Med Alliance SA

See all devices from M.A. Med Alliance SA →

Properties

  • Sterile
  • Incorporates Medicinal Product

Other properties (9)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No