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Venflon

EUDAMED

Class IIa (EU MDR)

Ref 393237

by Becton Dickinson Infusion Therapy Systems Inc.

Identity

Trade Name
Venflon EUDAMED
Device Name
BD Venflon™ Pro IV Cannula EUDAMED
Model / Reference
393237 EUDAMED

Identifiers

Primary DI / UDI-DI
30382903932376 EUDAMED
Basic UDI-DI
038290CPXPNDXWGX EUDAMED
Unit of Use DI
00382903932375 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
Hungary EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

Yes

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

Venflon by Becton Dickinson Infusion Therapy Systems Inc. — 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
US-MF-000017719
Authorised Representative
Becton Dickinson Ireland Limited IE-AR-000007610

Sources (1)

  • EUDAMED eb7ba94d-67f7-41e2-8e7f-29ea4dfd9e96 61 fields · synced Jul 9, 2026