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Nelaton catheters

EUDAMED

Class IIa (EU MDR)

Ref 30011Model Nelaton catheters

by Poly Medicure Limited

Identity

Trade Name
Nelaton catheters EUDAMED
Device Name
Nelaton catheters EUDAMED
Model / Reference
Nelaton catheters EUDAMED
30011 EUDAMED

Identifiers

Primary DI / UDI-DI
08902095300114 EUDAMED
Basic UDI-DI
890209530010DP EUDAMED
EMDN Code
U01010502 NELATON CATHETERS, NON SELF-LUBRICATING EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

Nelaton catheters by Poly Medicure Limited — 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
IN-MF-000043009
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 5c9d630f-f62e-4ce8-923d-a8a5918fda55 61 fields · synced Jul 30, 2026