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Callisto Medical Inhalation Cartridge

by Jupiter Research LLC.

Ref CM12nn-195XXXX

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08600073451CM12nnML Basic UDI-DI 00860007345173UDI-DIDate14 Jan 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Callisto Medical Inhalation Cartridge
Model / Reference
CM12nn-195XXXX
Primary DI / UDI-DI
00860007345173
Basic UDI-DI
08600073451CM12nnML
EMDN Code
R0680 Nebulisation and humidification systems - accessories not included in other classes
Device Class
Class I
EU market of registration
Portugal

Manufacturer details

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

Other devices from Jupiter Research LLC.

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