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SELUTION SLR™ 018 PTA Balloon Catheter

by M.A. Med Alliance SA EUDAMED

Active European Union

Ref SE18-070100

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07640278880404 Basic UDI-DIDate17 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

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.

Specification

EUDAMED

Device Name
SELUTION SLR™ PTA Balloon Catheter
Model / Reference
SE18-070100
Primary DI / UDI-DI
07640278880404
Basic UDI-DI
B-07640278880404
EMDN Code
C010402020199 PTA dilatation catheters - other
Device Class
Class III
Market of Registration
Germany

Manufacturer details

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

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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