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Vigi 3004

by Air Liquide Medical Systems S.A. EUDAMED

Active European Union

Ref AF301048

Regulatory status

as of 27 Oct 2026

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

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Vigi Line
Model / Reference
AF301048
Primary DI / UDI-DI
03700504302163
Basic UDI-DI
37005043VIGILINERT
Direct Marketing DI
03700504302163
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

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