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12li-A

EUDAMED

Class IIa (EU MDR)

Ref /Model 12L-ARef -

by Sonoscape Medical Corp.

Identity

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

Identifiers

Primary DI / UDI-DI
06945868604882 EUDAMED
06945868610470 EUDAMED
Basic UDI-DI
69458686P1001QJ EUDAMED
Direct Marketing DI
06945868604882 EUDAMED
06945868610470 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

12li-A 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 (2)

  • EUDAMED a8b47c84-f375-46b8-998f-ff161381430f 61 fields · synced Oct 6, 2026
  • EUDAMED 6988a3cc-3eff-4014-bc2e-c8709edb66f1 61 fields · synced May 16, 2026