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Combo Electrotherapy Device

EUDAMED

Class IIa (EU MDR)

Ref M101A-WH2Model Combo Electrotherapy Device

by Shenzhen Roundwhale Technology Co., Ltd.

Identity

Trade Name
Combo Electrotherapy Device EUDAMED
Device Name
Combo Electrotherapy Device EUDAMED
Model / Reference
Combo Electrotherapy Device EUDAMED
M101A-WH2 EUDAMED

Identifiers

Primary DI / UDI-DI
06971763600872 EUDAMED
Basic UDI-DI
697176360CE000173 EUDAMED
Direct Marketing DI
06971763600872 EUDAMED
EMDN Code
Z120622 MUSCLE STIMULATORS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Sweden 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

Combo Electrotherapy Device by Shenzhen Roundwhale 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-000021504
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 3f7f63ff-c99c-452b-b23e-7af684e6dd49 61 fields · synced May 29, 2026