Skip to content

ET Catheter

by Kitazato Corporation EUDAMED

Active European Union

Ref 223522

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number458223146ETCHW Basic UDI-DIDate30 Apr 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  • Withdrawn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
ET Catheter
Model / Reference
223522
Primary DI / UDI-DI
04580303267059
Basic UDI-DI
458223146ETCHW
EMDN Code
U08020102 Catheters for embryo transfer
Device Class
Class I
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
JP-MF-000018374
Authorised representative
BIOMEDICAL SUPPLY, S.L. ES-AR-000014358

Other devices from Kitazato Corporation

See all devices from Kitazato Corporation →

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