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BIOCATH Uriplan

by C. R. Bard, Inc. 25 variants

Ref D22655S14

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 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0801741QDEHEGITQ9 Basic UDI-DI 00801741186400UDI-DIDate28 Oct 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  • Withdrawn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
Biocath, Bardia PTFE, and Lubri-Sil - Foley Catheter Trays
Model / Reference
D22655S14
Primary DI / UDI-DI
00801741186400
Basic UDI-DI
0801741QDEHEGITQ9
EMDN Code
U0180 Urethral prostatic and bladder catheters - accessories
Device Class
Class IIb
Medical Purpose
The Latex Foley Catheter Tray is indicated for use in the drainage, collection and/or measurement of urine.

Manufacturer details

EUDAMED SRN
US-PR-000037901

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Properties

  • Sterile