Skip to content

Perio-Flush

by ARKONA Laboratorium Farmakologii Stomatologicznej Grzegorz Kalbarczyk 3 variants

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 linked in EUDAMED

A group certificate may exist

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 Number590443371TF0147F Basic UDI-DI 05904433711852UDI-DIDate11 Feb 2026RegisteredStatusActive

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.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Perio-flush / Parosin/ Perioactive
Primary DI / UDI-DI
05904433711852
Basic UDI-DI
590443371TF0147F
EMDN Code
Q019003, Q019006
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
PL-MF-000029550

Other devices from ARKONA Laboratorium Farmakologii Stomatologicznej Grzegorz Kalbarczyk

See all devices from ARKONA Laboratorium Farmakologii Stomatologicznej Grzegorz Kalbarczyk →

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