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NaviAid ABC

EUDAMED

Class IIa (EU MDR)

Ref 23-010Model AB-F

by SMART Medical Systems Ltd.

Identity

Trade Name
NaviAid ABC EUDAMED
Device Name
NaviAid AB Disposable EUDAMED
Model / Reference
AB-F EUDAMED
23-010 EUDAMED

Identifiers

Primary DI / UDI-DI
07290018671726 EUDAMED
Basic UDI-DI
7290018671ABEM EUDAMED
EMDN Code
G0380 DIGESTIVE ENDOSCOPY DEVICES - ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED

Clinical & Handling

Sterile

No

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: Gastro-urological guidewire, single-use

NaviAid ABC by Smart Medical Systems Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Gastro-urological guidewire, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IL-MF-000011336
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED c4472a4f-744e-48ea-9296-adc08af86a25 61 fields · synced Oct 6, 2026