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Hydrophilic Nelaton Catheter

EUDAMED

Class IIa (EU MDR)

Ref WHM14TModel WHF10

by Integral Medical Products Co., Ltd.

Identity

Trade Name
KONTICUR® Kath H+M EUDAMED
Device Name
Hydrophilic Nelaton Catheter EUDAMED
Hydrophilic Nelaton Catheter EUDAMED
Model / Reference
WHM14T EUDAMED
WHF10 EUDAMED

Identifiers

Primary DI / UDI-DI
06970675357041 EUDAMED
Basic UDI-DI
B-06970675357041 EUDAMED
697067535IMP2ASNNNSNCH1YG 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

Hydrophilic Nelaton Catheter by Integral Medical Products Co., Ltd. — Class IIa — MDR, MDD — 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

European Union Active

CE/MDD

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Manufacturer

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

Sources (2)

  • EUDAMED 0a11c752-58ae-4bdf-9db1-cfc76a39447c 61 fields · synced Jul 28, 2026
  • EUDAMED 01de5c46-2e83-46ce-9add-a2b28872defc 61 fields · synced Jul 28, 2026