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Reusable Heated Wire Delivery Circuit (SLE4000/SLE5000/SLE6000)

by SLE Ltd EUDAMED

Active European Union

Ref N2391/50

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05051380001106 Basic UDI-DIDate21 Oct 2026RegisteredStatusActive

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  • Withdrawn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
Reusable Patient Delivery Circuits
Model / Reference
N2391/50
Primary DI / UDI-DI
05051380001106
Basic UDI-DI
B-05051380001106
EMDN Code
R02010401 Cpap circuits
Device Class
Class IIa
Market of Registration
Latvia

Manufacturer details

EUDAMED SRN
GB-MF-000004155
Authorised representative
Advena Limited MT-AR-000000234

Other devices from SLE Ltd

See all devices from SLE Ltd →

Properties

Show properties
Other properties (11)
  • Sterile: No
  • 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