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SeQure

by LifeTech Scientific (Europe) B.V. EUDAMED

Active European Union

Ref LE-SP-25

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08720214007771 Basic UDI-DIDate2 Aug 2023RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
SeQure™ Snare System
Model / Reference
LE-SP-25
Primary DI / UDI-DI
08720214007771
Basic UDI-DI
B-08720214007771
EMDN Code
C010280 Central venous catheters - accessories
Device Class
Class IIa
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
NL-MF-000005742

Other devices from LifeTech Scientific (Europe) B.V.

See all devices from LifeTech Scientific (Europe) B.V. →

Properties

  • Sterile

Other properties (10)

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