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Female catheter

by Changzhou Weite Medical Equipment Co., Ltd. EUDAMED

Active European Union

Ref WT002-03-01Model 5,6,8,10,12,14,16,18,20,22

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697594680JSCZWTnelatonWA Basic UDI-DIDate9 Dec 2022RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Nelaton catheter
Model / Reference
5, 6, 8, 10, 12, 14, 16, 18, 20, 22, WT002-03-01
Primary DI / UDI-DI
26975946801128, 36975946801163
Basic UDI-DI
697594680JSCZWTnelatonWA
EMDN Code
U01010502 Nelaton catheters, non self-lubricating
Device Class
Class IIa
Market of Registration
Denmark

Manufacturer details

EUDAMED SRN
CN-MF-000029258
Authorised representative
Caretechion GmbH DE-AR-000005946

Other devices from Changzhou Weite Medical Equipment Co., Ltd.

See all devices from Changzhou Weite Medical Equipment Co., Ltd. →

Properties

Show properties
  • Sterile
  • CMR Substance
  • Endocrine Disruptor
Other properties (10)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No