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Lifeflow Efa®

by Medical Products Research Italy EUDAMED

Ref MPR904Model LIFEFLOW EFA®

EMDN Z1203019099

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-ITMF000025583HFLXX03ZT Basic UDI-DIDate13 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Device Name
High flow oxygen therapy
Model / Reference
LIFEFLOW EFA®, MPR904
Primary DI / UDI-DI
D-ITMF000025583HFLXX03ZT
Basic UDI-DI
B-ITMF000025583HFLXX03ZT
EMDN Code
Z1203019099 Various instruments for anaesthesia and pulmonary ventilation support – other
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000025583

Other devices from Medical Products Research

See all devices from Medical Products Research →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED D-ITMF000025583HFLXX03ZT|B-ITMF000025583HFLXX03ZT 61 fields · synced 25 Oct 2026