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Anoscope

by Yuhuan City Shengbo Mould Manufacturing Co., Ltd. 10 variants

Ref SY101W-MModel M

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06972903332400 Basic UDI-DI 06972903332400UDI-DIDate9 Jun 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Anoscope
Model / Reference
M, SY101W-M
Primary DI / UDI-DI
06972903332400
Basic UDI-DI
B-06972903332400
EMDN Code
G02060301 Anoscopes
Device Class
Class I
EU market of registration
France

Manufacturer details

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

Other devices from Yuhuan City Shengbo Mould Manufacturing Co., Ltd.

See all devices from Yuhuan City Shengbo Mould Manufacturing Co., Ltd. →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No