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MRX003-T10 DPI; Dry Powder Inhaler (DPI)

by Phargentis SA

Ref MRX003-R

Active European Union

CE MDD

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-MRX003-T104Z Basic UDI-DI D-MRX003-T104ZUDI-DIDate26 Jun 2024RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
MRX003-T10 DPI; Dry Powder Inhaler (DPI)
Model / Reference
MRX003-R
Primary DI / UDI-DI
D-MRX003-T104Z
Basic UDI-DI
B-MRX003-T104Z
EMDN Code
R900901 Inhalers
Models / Variants
Device Class
Class I
EU market of registration
Norway

Manufacturer details

EUDAMED SRN
CH-MF-000023068
Authorised representative
ProPharma Group The Netherlands BV NL-AR-000020273

From the manufacturer

Manufacturer's product page: Albanian

Properties

  • Administering Medicine

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No