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Anoscope

EUDAMED

Class I (EU MDR)

Ref SY101W-MModel M

by Yuhuan City Shengbo Mould Manufacturing Co., Ltd.

Identity

Device Name
Anoscope EUDAMED
Model / Reference
M EUDAMED
SY101W-M EUDAMED

Identifiers

Primary DI / UDI-DI
26972903332404 EUDAMED
Basic UDI-DI
B-26972903332404 EUDAMED
EMDN Code
G02060301 ANOSCOPES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Anoscope by Yuhuan City Shengbo Mould Manufacturing Co., Ltd. — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000036867
Authorised Representative
Prolinx GmbH DE-AR-000005129

Sources (1)

  • EUDAMED 5ed5099d-8611-469c-92cc-f4dd27a9d08f 61 fields · synced Jun 19, 2026