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NAQI Ultrason Gel 500ml

EUDAMED

Class I (EU MDR)

Ref US500

by Naqi NV

Identity

Trade Name
NAQI Ultrason Gel 500ml EUDAMED
Device Name
Ultrason gel EUDAMED
Model / Reference
US500 EUDAMED

Identifiers

Primary DI / UDI-DI
05425029890190 EUDAMED
Basic UDI-DI
542502989USUN EUDAMED
Direct Marketing DI
05425029890190 EUDAMED
EMDN Code
Z11040185 ULTRASOUND SCANNERS - CONSUMABLES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium 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

NAQI Ultrason Gel 500ml by Naqi NV — Class I — 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

Manufacturer
Naqi NV
EUDAMED SRN
BE-MF-000001241

Sources (1)

  • EUDAMED a506d160-b180-4083-a41c-83a6a3f9f8c9 61 fields · synced Jun 18, 2026