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7p-A

EUDAMED

Class IIa (EU MDR)

Ref -Model 7P-A

by Sonoscape Medical Corp.

Identity

Trade Name
7P-A EUDAMED
Device Name
Ultrasonic Transducer EUDAMED
Model / Reference
7P-A EUDAMED
- EUDAMED

Identifiers

Primary DI / UDI-DI
06945868608408 EUDAMED
Basic UDI-DI
69458686P1011QM EUDAMED
Direct Marketing DI
06945868608408 EUDAMED
EMDN Code
Z110402010301 TRANSCUTANEOUS ULTRASOUND SECTOR PROBES (PHASED ARRAY), TWO–DIMENSIONAL EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands 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

7p-A by Sonoscape Medical Corp. — 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

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Manufacturer

EUDAMED SRN
CN-MF-000009623
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 5ba5bfad-67e8-4f86-841d-241c03718705 61 fields · synced Oct 7, 2026