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The Tulip

by Gynétics Medical Products nv Belgium EUDAMED

Ref #4000 The Tulip EMDN U08020102

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number540700389ETC012D Basic UDI-DIDate28 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • BE26/00000093 Issued

    Quality management system EU MDR

    Notified body
    Notified body 1639
    Issued
    1 Apr 2026
    Expires
    1 Apr 2031

Specification

EUDAMED · synced 23 Oct 2026

Device Name
#4000 The Tulip
Model / Reference
#4000 The Tulip
Primary DI / UDI-DI
05407003890372
Basic UDI-DI
540700389ETC012D
Direct Marketing DI
05407003890372
EMDN Code
U08020102 Catheters for embryo transfer
Device Class
Class I
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
BE-MF-000024832

Other devices from Gynétics Medical Products nv

See all devices from Gynétics Medical Products nv →

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 440badb6-9651-48f0-9114-e69fd7dd4743 61 fields · synced 23 Oct 2026