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Sinuscope

EUDAMED

Class I (EU MDR)

Ref B703AFModel B005AC、B305AC、B004AC、B304AC、B704AC、B003AE、B303AE、B703AE、B003AF、B303AF、B703AF

by Wuzhou Aokace Technology Co., Ltd.

Identity

Trade Name
Sinuscope EUDAMED
Device Name
Sinuscope EUDAMED
Model / Reference
B005AC、B305AC、B004AC、B304AC、B704AC、B003AE、B303AE、B703AE、B003AF、B303AF、B703AF EUDAMED
B703AF EUDAMED

Identifiers

Primary DI / UDI-DI
06975465800301 EUDAMED
Basic UDI-DI
697546580SBAERP EUDAMED
EMDN Code
Z12021008 RHINOSCOPES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Sinuscope by Wuzhou Aokace Technology 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-000027213
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED a38a847f-4543-4a1c-8bcf-2b6abebac267 61 fields · synced Jun 19, 2026