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Integra

EUDAMED

Class IIa (EU MDR)

Ref GS-3231 KAD

by Romsons Group Private Limited

Identity

Trade Name
INTEGRA EUDAMED
Device Name
INTRAVENOUS CANNULA EUDAMED
Model / Reference
GS-3231 KAD EUDAMED

Identifiers

Primary DI / UDI-DI
08907265010602 EUDAMED
Basic UDI-DI
8907265C001YH EUDAMED
EMDN Code
C0101010101 PERIPHERAL I.V. CATHETERS, W/O SAFETY SYSTEMS, WITH 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

Integra 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 b7360ae9-9e23-4c47-9e4f-04e3af4d6e4b 61 fields · synced Aug 3, 2026