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Medical Mart

by Αριστειδης Παρδαλης Του Γεωργιου EUDAMED

Active European Union

Ref 15.01.01

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number521301209ToPD7 Basic UDI-DIDate26 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Device Name
Χαρτοβαμβακας Αα
Model / Reference
15.01.01
Primary DI / UDI-DI
05213012090791
Basic UDI-DI
521301209ToPD7
EMDN Code
T0306 Patient protection devices during clinical procedures
Device Class
Class I
Market of Registration
Greece

Manufacturer details

EUDAMED SRN
EL-MF-000056062

Other devices from Αριστειδης Παρδαλης Του Γεωργιου

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