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Otoscope

by Shenzhen Yipincheng Technology Co., Ltd. 23 variants

Ref X8Model X6, Q9, Q10, Q11, Q12, Q13, Q15, Q16, Q17, Q18, X8, FIND T, R3, N3Pro, B8, S2Pro, S2, B2, R2, B6,R3-G ,B5,B5pro

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697387876086T3 Basic UDI-DI 06973878760106UDI-DIDate10 Aug 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Otoscope
Model / Reference
X6, Q9, Q10, Q11, Q12, Q13, Q15, Q16, Q17, Q18, X8, FIND T, R3, N3Pro, B8, S2Pro, S2, B2, R2, B6, R3-G, B5, B5pro
Primary DI / UDI-DI
06973878760106
Basic UDI-DI
697387876086T3
EMDN Code
Q030499 Otology devices - other
Device Class
Class I
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
CN-MF-000057543
Authorised representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Other devices from Shenzhen Yipincheng Technology Co., Ltd.

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Properties

Other properties (13)

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