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Ultrasound Probes

EUDAMED

Class IIa (EU MDR)

Ref P5-1S

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

Identity

Trade Name
ULTRASOUND PROBES EUDAMED
Device Name
ULTRASOUND PROBES EUDAMED
Model / Reference
P5-1S EUDAMED

Identifiers

Primary DI / UDI-DI
06974676310111 EUDAMED
Basic UDI-DI
697467631PhasedM8 EUDAMED
Direct Marketing DI
06974676310111 EUDAMED
EMDN Code
Z110402010101 TWO–DIMENSIONAL LINEAR–ARRAY TRANSCUTANEOUS ULTRASOUND PROBES 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: Extracorporeal ultrasound imaging transducer, hand-held

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

Similar devices

Also classified as Extracorporeal ultrasound imaging transducer, hand-held.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

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

Sources (1)

  • EUDAMED 9250d70c-2b9e-4912-9700-6dce8e7faed5 61 fields · synced Oct 8, 2026