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L742

EUDAMED

Class IIa (EU MDR)

Ref -Model 12L-A

by Sonoscape Medical Corp.

Identity

Trade Name
L742 EUDAMED
Device Name
Ultrasonic Transducer EUDAMED
Model / Reference
12L-A EUDAMED
- EUDAMED

Identifiers

Primary DI / UDI-DI
06945868610456 EUDAMED
Basic UDI-DI
69458686P1001QJ EUDAMED
Direct Marketing DI
06945868610456 EUDAMED
EMDN Code
Z110402010101 TWO–DIMENSIONAL LINEAR–ARRAY TRANSCUTANEOUS ULTRASOUND PROBES 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

Category: Extracorporeal ultrasound imaging transducer, hand-held

L742 by Sonoscape Medical Corp. — 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-000009623
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED b4be0baa-280b-4d74-af70-ab1d256228ad 61 fields · synced Jun 17, 2026