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Single Use Digital Flexible Ureteroscope w/ Pressure Monitoring

by Anhui Happiness Workshop Medical Instruments Co., Ltd 6 variants

Ref HUS-M102S

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6972498490100F5 Basic UDI-DI 06972498493531UDI-DIDate22 Aug 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Digital Flexible Ureteroscope
Model / Reference
HUS-M102S
Primary DI / UDI-DI
06972498493531
Basic UDI-DI
6972498490100F5
Direct Marketing DI
06972498493531
EMDN Code
Z12020713 Ureterorenoscopes
Device Class
Class IIa
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
CN-MF-000007232
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Anhui Happiness Workshop Medical Instruments Co., Ltd

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Properties

  • Sterile

Other properties (12)

  • 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