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Rectal Catheter

by Changzhou Weite Medical Equipment Co., Ltd. EUDAMED

Active European Union

Ref CC Rev. 7.1: 2023-01-23Model 22,24,25,26,28,30,32,34,36

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697594680JSCZWTrectalZU Basic UDI-DIDate12 Feb 2023RegisteredStatusActive

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  • Withdrawn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
Rectal tube
Model / Reference
22, 24, 25, 26, 28, 30, 32, 34, 36, CC Rev. 7.1: 2023-01-23
Primary DI / UDI-DI
26975946806024, 16975946806010
Basic UDI-DI
697594680JSCZWTrectalZU
EMDN Code
G020301 Rectal tubes
Device Class
Class I
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