Skip to content

Revitalair 430 by Biobarica

by Oxavita SRL EUDAMED

Active European Union

Ref 430

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-B878REVITALAIR430SL Basic UDI-DIDate8 Jun 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  • Withdrawn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

Model / Reference
430
Primary DI / UDI-DI
B878REVITALAIR430SL
Basic UDI-DI
B-B878REVITALAIR430SL
EMDN Code
Z120308 Hyperbaric chambers
Device Class
Class IIb
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
AR-MF-000001878
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Oxavita SRL

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