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X-Ray Disc

by Polident d.o.o. Industrija dentalnih proizvodov 7 variants

Ref PMMR.509

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++EPOLQ01992A Basic UDI-DI +EPOLPMMR5090KUDI-DIDate17 Apr 2025RegisteredStatusActive

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  • Withdrawn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

Model / Reference
PMMR.509
Primary DI / UDI-DI
+EPOLPMMR5090K
Basic UDI-DI
++EPOLQ01992A
Direct Marketing DI
+EPOLPMMR5090K
EMDN Code
Q0199 Odontology devices - other
Device Class
Class I
EU market of registration
Slovenia

Manufacturer details

EUDAMED SRN
SI-MF-000000740

Other devices from Polident d.o.o. Industrija dentalnih proizvodov

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    Class IIa

  • K-30 S

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  • Polirepar S

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  • Policold

    Class IIa

  • Polirepar S

    Class IIa

  • K-30 S

    Class IIa

See all devices from Polident d.o.o. Industrija dentalnih proizvodov →

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