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Rectal Catheter

by Changzhou Weite Medical Equipment Co., Ltd. 4 variants

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

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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 Number697594680JSCZWTrectalZU Basic UDI-DI 26975946806048UDI-DIDate12 Feb 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

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
26975946806048
Basic UDI-DI
697594680JSCZWTrectalZU
EMDN Code
G020301 Rectal tubes
Device Class
Class I
EU 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

  • 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