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KONTICUR® Kath H+F

EUDAMED

Class IIa (EU MDR)

Ref WHF14Model WHF10

by Integral Medical Products Co., Ltd.

Identity

Trade Name
KONTICUR® Kath H+F EUDAMED
Device Name
Hydrophilic Nelaton Catheter EUDAMED
Hydrophilic Nelaton Catheter EUDAMED
Model / Reference
WHF10 EUDAMED
WHF14 EUDAMED

Identifiers

Primary DI / UDI-DI
06970675359762 EUDAMED
Basic UDI-DI
697067535IMP2ASNNNSNCH1YG EUDAMED
B-06970675359762 EUDAMED
EMDN Code
U01010501 NELATON CATHETERS, SELF-LUBRICATING EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

KONTICUR® Kath H+F by Integral Medical Products Co., Ltd. — Class IIa — MDD, 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/MDD

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000009217
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (2)

  • EUDAMED 50c09d35-1482-4542-8f4a-abae0a03fd18 61 fields · synced Jul 11, 2026
  • EUDAMED 16833cf9-682e-4c4b-b689-e71cf45b4041 61 fields · synced Jul 11, 2026