← Back to catalogue

Plusflon

EUDAMED

Class IIa (EU MDR)

Ref MIL/16/V/2018Model Sterile IV Cannula - 14G

by Mediplus (India) Limited

Identity

Trade Name
PLUSFLON EUDAMED
Device Name
Sterile IV Cannula EUDAMED
Model / Reference
Sterile IV Cannula - 14G EUDAMED
MIL/16/V/2018 EUDAMED

Identifiers

Primary DI / UDI-DI
08906025300847 EUDAMED
Basic UDI-DI
890602530IVCANNULAK6 EUDAMED
Secondary DI
18906025300844 EUDAMED
Direct Marketing DI
08906025300847 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
Estonia 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

Plusflon by Mediplus (India) 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
IN-MF-000007279
Authorised Representative
mdi Europa GmbH DE-AR-000006218

Sources (1)

  • EUDAMED 8c67d682-5f14-4e5c-9684-6230a16342ba 61 fields · synced Aug 1, 2026