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ME100

by Ca-Mi S.R.L. EUDAMED

Active European Union

Ref REF RE 300240/04Model AEROSOL THERAPY EQUIPMENT

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805461910Z121590023V Basic UDI-DIDate12 Aug 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Specification

EUDAMED

Device Name
Aerosol Therapy Equipment
Model / Reference
AEROSOL THERAPY EQUIPMENT, REF RE 300240/04
Primary DI / UDI-DI
08054619108338
Basic UDI-DI
805461910Z121590023V
Direct Marketing DI
08054619108338
EMDN Code
Z12159002 Aerosol equipment
Device Class
Class IIa
Market of Registration
Croatia

Manufacturer details

EUDAMED SRN
IT-MF-000020076

Other devices from Ca-Mi S.R.L.

See all devices from Ca-Mi S.R.L. →

Properties

  • Administering Medicine

Other properties (12)

  • 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
  • Measuring Function: No
  • Incorporates Medicinal Product: No