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Oropharyngeal Airway

EUDAMED

Class I (EU MDR)

Ref 830020CModel Z40、Z50、Z60、Z70、Z80、Z90、Z100、Z110、Z120、Z40~Z110、Z40~Z120

by Xiamen Compower Medical Tech. Co., Ltd.

Identity

Trade Name
Oropharyngeal Airway EUDAMED
Device Name
Oropharyngeal Airway EUDAMED
Model / Reference
Z40、Z50、Z60、Z70、Z80、Z90、Z100、Z110、Z120、Z40~Z110、Z40~Z120 EUDAMED
830020C EUDAMED

Identifiers

Primary DI / UDI-DI
06946430419958 EUDAMED
Basic UDI-DI
694643043130801N2 EUDAMED
EMDN Code
R010102 GUEDEL AIRWAY TUBES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Oropharyngeal Airway by Xiamen Compower Medical Tech. Co., Ltd. — Class I — 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-000011703
Authorised Representative
Sungo Cert GmbH DE-AR-000010869

Sources (1)

  • EUDAMED b7221602-fb4c-4289-85f3-d0be90dbe6ea 61 fields · synced Jun 19, 2026