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Liquick Base, Intermittent Catheter

EUDAMED

Class I (EU MDR)

Ref 631012 CH 12

by Teleflex Medical

Identity

Trade Name
Liquick Base, Intermittent Catheter EUDAMED
Device Name
Liquick Base/Solo EUDAMED
Model / Reference
631012 CH 12 EUDAMED

Identifiers

Primary DI / UDI-DI
14026704733269 EUDAMED
Basic UDI-DI
08019020000000000000142KD EUDAMED
EMDN Code
U01010501 NELATON CATHETERS, SELF-LUBRICATING EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Intermittent urethral drainage catheter, non-antimicrobial, single-use

Liquick Base, Intermittent Catheter by Teleflex Medical — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent urethral drainage catheter, non-antimicrobial, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Teleflex Medical
EUDAMED SRN
IE-MF-000015868

Sources (1)

  • EUDAMED 3a3d0f90-8d4e-421b-ada9-e2a80e821287 61 fields · synced Jun 19, 2026