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Interflow Blender - Lithuania (Packaging)

by SLE Ltd United Kingdom EUDAMED

Ref 7210017 EMDN Z1203019080

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05051380007665 Basic UDI-DIDate27 Aug 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  • Withdrawn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 · synced 23 Oct 2026

Device Name
Interflow Blender
Model / Reference
7210017
Primary DI / UDI-DI
05051380007665
Basic UDI-DI
B-05051380007665
EMDN Code
Z1203019080 Various instruments for anaesthesia and pulmonary ventilation support - hardware accessories
Device Class
Class IIb
Market of Registration
Belgium

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 & raw data

Show properties, registry sources and raw records
  • Administering Medicine
  • Measuring Function
Other properties (9)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 832ca36f-f1d4-4cf8-aa88-646283d14b90 61 fields · synced 23 Oct 2026