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Soundway

EUDAMED

Class IIa (EU MDR)

Ref C0201Model Standard

by Ningbo Shengyurui Medical Appliances Co., Ltd.

Identity

Trade Name
Soundway EUDAMED
Device Name
Nasal Cannula EUDAMED
Model / Reference
Standard EUDAMED
C0201 EUDAMED

Identifiers

Primary DI / UDI-DI
06945099394521 EUDAMED
Basic UDI-DI
69450993NOCSTD01JD EUDAMED
Secondary DI
46945099394529 EUDAMED
Direct Marketing DI
06945099394521 EUDAMED
EMDN Code
R0301020301 OXYGEN THERAPY STANDARD NASAL CANNULAS (GOGGLES) EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Soundway by Ningbo Shengyurui Medical Appliances 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-000026643
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 9fbcbbf2-26a5-4070-b6a2-83635b43f550 61 fields · synced Jun 19, 2026