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3 Way Rusch Gold 30cc

by Teleflex Medical Private Limited 6 variants

Ref 183430-CH22

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 Number08019020000000000000331KJ Basic UDI-DI 14026704917881UDI-DIDate21 Jul 2026RegisteredStatusActive

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  • Withdrawn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
2 Way & 3 Way Latex Foley Catheter
Model / Reference
183430-CH22
Primary DI / UDI-DI
14026704917881
Basic UDI-DI
08019020000000000000331KJ
EMDN Code
U010299 Urethral prostatic and bladder catheters, with balloon - other
Device Class
Class IIa
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
IN-MF-000024260
Authorised representative
Teleflex Medical IE-AR-000015869

Other devices from Teleflex Medical Private Limited

See all devices from Teleflex Medical Private Limited →

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