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Shock Wave Therapy System

EUDAMED

Class IIa (EU MDR)

Ref NAModel LC-560,LC-570,LC-310,LC-320

by Shenzhen Lifotronic Technology Co., Ltd.

Identity

Device Name
Shock Wave Therapy System EUDAMED
Model / Reference
LC-560,LC-570,LC-310,LC-320 EUDAMED
NA EUDAMED

Identifiers

Primary DI / UDI-DI
06975984061405 EUDAMED
Basic UDI-DI
6970341680111601H8 EUDAMED
Direct Marketing DI
06975984061405 EUDAMED
EMDN Code
Z12139001 SHOCK WAVE THERAPY EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Ireland 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

Shock Wave Therapy System by Shenzhen Lifotronic Technology Co., Ltd. — Class IIa — 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-000005654
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (2)

  • EUDAMED 14a17f50-aab0-4ea7-8d11-9b12c5281da3 61 fields · synced Jun 18, 2026
  • EUDAMED 14a17f50-aab0-4ea7-8d11-9b12c5281da3-1 61 fields · synced Jun 11, 2026