← Back to catalogue

Ultrasound Diagnostic System

EUDAMED

Class IIa (EU MDR)

Ref Danus 10Pro

by Focus&Fusion Healthcare (Hangzhou) Co., Ltd

Identity

Trade Name
Ultrasound Diagnostic System EUDAMED
Device Name
Ultrasound Diagnostic System EUDAMED
Model / Reference
Danus 10Pro EUDAMED

Identifiers

Primary DI / UDI-DI
16974676310569 EUDAMED
Basic UDI-DI
697467631FF060702K4 EUDAMED
Direct Marketing DI
16974676310569 EUDAMED
EMDN Code
Z11040104 MULTIDISCIPLINARY ULTRASOUND SCANNERS (INTERNAL AND CARDIOLOGY, ETC.) 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Ultrasound Diagnostic System by Focus&Fusion Healthcare (Hangzhou) Co., Ltd — Class IIa — CE/MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000017932
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED f0dbb267-edd0-4ea7-86d3-8c77b9bd7a26 61 fields · synced Oct 7, 2026