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Nelaton Catheter

EUDAMED

Class IIa (EU MDR)

Ref GS-1004F

by Romsons Group Private Limited

Identity

Trade Name
NELATON CATHETER EUDAMED
Device Name
NELATON CATHETER EUDAMED
Model / Reference
GS-1004F EUDAMED

Identifiers

Primary DI / UDI-DI
08907265000351 EUDAMED
Basic UDI-DI
8907265A002Y5 EUDAMED
EMDN Code
U01010502 NELATON CATHETERS, NON SELF-LUBRICATING EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria 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 Catheter by Romsons Group Private 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-000036506
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED b1a50929-9e39-4e6e-bba5-5e0d191fb606 61 fields · synced Jul 31, 2026