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Embotrap Ii

EUDAMED

Class III (EU MDR)

Ref ET-007-521

by Neuravi Limited

Identity

Trade Name
EMBOTRAP II EUDAMED
Model / Reference
ET-007-521 EUDAMED

Identifiers

Primary DI / UDI-DI
D-IEMF00000761200000258 EUDAMED
Basic UDI-DI
B-IEMF00000761200000258 EUDAMED
EMDN Code
C019010 INTRAVASCULAR RECANALISATION SYSTEMS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Ireland 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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Vascular graft tunneller

Embotrap Ii by Neuravi Limited — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Vascular graft tunneller.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Neuravi Limited
EUDAMED SRN
IE-MF-000007612

Sources (1)

  • EUDAMED bb48c6e5-7359-4dca-b197-f6930eb7ce47 61 fields · synced May 23, 2026