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Vigi Line X3

by Air Liquide Medical Systems S.A. France EUDAMED

Ref AF301038

EMDN Z120309

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number37005043VIGILINERT Basic UDI-DIDate1 Oct 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Vigi Line
Model / Reference
AF301038
Primary DI / UDI-DI
03700504302149
Basic UDI-DI
37005043VIGILINERT
Direct Marketing DI
03700504302149
EMDN Code
Z120309 Medical/medicinal gas pipeline systems and related accessories
Device Class
Class I
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000003649

Other devices from Air Liquide Medical Systems S.A.

See all devices from Air Liquide Medical Systems S.A. →

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED c80e539a-c0d0-4223-abf7-74b0ac07a065 61 fields · synced 24 Oct 2026