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AD Hydrophilic Nelaton Catheter

EUDAMED

Class IIa (EU MDR)

Ref ADM08WT

by Integral Medical Products Co., Ltd.

Identity

Device Name
AD Hydrophilic Nelaton Catheter EUDAMED
Model / Reference
ADM08WT EUDAMED

Identifiers

Primary DI / UDI-DI
06970675351704 EUDAMED
Basic UDI-DI
697067535IMP2ASNNNSADS1WT 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

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

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

Sources (1)

  • EUDAMED 4ef270a1-36d2-47b5-8612-a4f9a11383d4 61 fields · synced Jul 14, 2026