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Sim Micro Cannula Polyshaft

by Med Europe European Medical Supplies SRL 16 variants

Ref PD-DS-1038

Active European Union

CE MDR

Valid until

11 May 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier ICIM S.P.A.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0425-MDR-030029-02 Date11 Jun 2026IssuedStatusActive expires 11 May 2028

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 0425-MDR-030029-02 Active

    Quality management system EU MDR

    Certifier
    ICIM S.P.A. 0425
    Issued
    11 Jun 2026
    Expires
    11 May 2028

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Sim Micro Cannula
Model / Reference
PD-DS-1038
Primary DI / UDI-DI
08033609522958
Basic UDI-DI
803360952CANNULEG9
EMDN Code
A06010103 Cannulas and tips for aspiration and irrigation, single-use
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IT-MF-000026962

From the manufacturer

Manufacturer's product page: ENT Sim Micro Cannula POLYSHAFT

Other devices from Med Europe European Medical Supplies SRL

See all devices from Med Europe European Medical Supplies SRL →

Properties

  • Sterile

Other properties (12)

  • 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