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Curan Plain

by Curan Medical BV 12 variants

Ref M08Model Curan Uncoated Plain Male and Female - PVC

Active European Union

CE MDR

Valid until

16 Jan 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SGS Belgium NV

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 NumberBE26/00000017 Date9 Apr 2026IssuedStatusActive expires 16 Jan 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • BE26/00000017 Restricted

    Quality management system EU MDR

    Certifier
    SGS Belgium NV 1639
    Issued
    9 Apr 2026
    Expires
    16 Jan 2031
    Reason
    Other

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
Curan Uncoated Plain Male and Female - PVC, M08
Primary DI / UDI-DI
08718657210599
Basic UDI-DI
871865721PVC-PLRZ
Direct Marketing DI
08718657210599
EMDN Code
U01010502 Nelaton catheters, non self-lubricating
Device Class
Class I
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
NL-MF-000022827

Other devices from Curan Medical BV

See all devices from Curan Medical BV →

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