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Flexiport

EUDAMED

Class IIa (EU MDR)

Ref 110801

by Invent Bio-Med Pvt Ltd

Identity

Trade Name
FLEXIPORT EUDAMED
Device Name
2 Port / 3 Port / 4 Port Manifold EUDAMED
Model / Reference
110801 EUDAMED

Identifiers

Primary DI / UDI-DI
08906026860005 EUDAMED
Basic UDI-DI
890602686POMRL EUDAMED
Direct Marketing DI
08906026860005 EUDAMED
EMDN Code
A0799 ADAPTERS, CONNECTORS, RAMPS, STOPCOCKS, CAPS - OTHER EUDAMED

Classification

Device Class
Class IIa 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

Flexiport by Invent Bio-Med Pvt Ltd — 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-000028640
Authorised Representative
mdi Europa GmbH DE-AR-000006218

Sources (1)

  • EUDAMED 23435845-174c-45e6-a332-481b26b259e1 61 fields · synced Jun 18, 2026