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BenQ

EUDAMED

Class IIa (EU MDR)

Ref 9J.2SG21.902Model InnoSight/T3300/H1300

by Qisda Corporation

Identity

Trade Name
BenQ EUDAMED
Device Name
Diagnostic Ultrasound System EUDAMED
Model / Reference
InnoSight/T3300/H1300 EUDAMED
9J.2SG21.902 EUDAMED

Identifiers

Primary DI / UDI-DI
04719873009282 EUDAMED
Basic UDI-DI
471987300VIVAPRO5J EUDAMED
Direct Marketing DI
04719873009282 EUDAMED
EMDN Code
Z11040103 PORTABLE ULTRASOUND SCANNERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Ireland 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

BenQ by Qisda Corporation — 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

Manufacturer
Qisda Corporation
EUDAMED SRN
TW-MF-000010709
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 7fc7e3b8-0f2c-4f8d-ae8c-009da120043f 61 fields · synced May 23, 2026