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Curaleaf

by Jupiter Research LLC. United States EUDAMED

Ref PM2033-085030-RPModel PM2033-00XX-RP

EMDN R060102

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08600073451PM2033RPZR Basic UDI-DIDate6 Sep 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Que Medical Inhalation Device
Model / Reference
PM2033-00XX-RP, PM2033-085030-RP
Primary DI / UDI-DI
00860007345111
Basic UDI-DI
08600073451PM2033RPZR
EMDN Code
R060102 Hot nebulisation systems
Device Class
Class IIa
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
US-MF-000032604
Authorised representative
Inter Scientific S.L. ES-AR-000027516

Other devices from Jupiter Research LLC.

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 92b72b09-a8ab-4880-84c6-6b815d4a24a1 61 fields · synced 22 Oct 2026