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Single Use Digital Flexible Ureteroscope (7.5F)

EUDAMED

Class IIa (EU MDR)

Ref HUS-T105R

by Anhui Happiness Workshop Medical Instruments Co., Ltd

Identity

Trade Name
Single Use Digital Flexible Ureteroscope (7.5F) EUDAMED
Device Name
Digital Flexible Ureteroscope EUDAMED
Model / Reference
HUS-T105R EUDAMED

Identifiers

Primary DI / UDI-DI
06972498490363 EUDAMED
Basic UDI-DI
6972498490100F5 EUDAMED
Direct Marketing DI
06972498490363 EUDAMED
EMDN Code
Z12020713 URETERORENOSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Portugal EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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

Category: Flexible video ureteroscope, single-use

Single Use Digital Flexible Ureteroscope (7.5F) by Anhui Happiness Workshop Medical Instruments Co., Ltd — Class IIa — MDR — listed in EUDAMED

Similar devices

Also classified as Flexible video ureteroscope, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

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

Sources (1)

  • EUDAMED f4c7a246-d79d-4c72-96ed-4cc67a75c267 61 fields · synced Jun 18, 2026