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Ready to use Hydrophilic Nelaton Catheter

EUDAMED

Class IIa (EU MDR)

Ref RHMC08TE

by Integral Medical Products Co., Ltd.

Identity

Device Name
Ready to use Hydrophilic Nelaton Catheter EUDAMED
Model / Reference
RHMC08TE EUDAMED

Identifiers

Primary DI / UDI-DI
06970675358345 EUDAMED
Basic UDI-DI
697067535IMP2ASNNNSRTU25D EUDAMED
EMDN Code
U01010601 TIEMANN 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

Ready to use Hydrophilic Nelaton Catheter by Integral Medical Products Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

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 (1)

  • EUDAMED 22d07702-ddb5-4738-bf3d-926a533bab82 61 fields · synced Jul 18, 2026