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Neo Cath-2

EUDAMED

Class IIa (EU MDR)

Ref GS-3030

by Romsons Group Private Limited

Identity

Trade Name
NEO CATH-2 EUDAMED
Device Name
INTRAVENOUS CANNULA EUDAMED
Model / Reference
GS-3030 EUDAMED

Identifiers

Primary DI / UDI-DI
08907265303001 EUDAMED
Basic UDI-DI
8907265C001YH EUDAMED
EMDN Code
C0101010102 PERIPHERAL I.V. CATHETERS, W/O SAFETY SYSTEMS, W/O INJECTION VALVES 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Neo Cath-2 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 f36f9d44-38eb-46f9-a6f5-2fe6a501cec3 61 fields · synced Jul 31, 2026