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Single Use Digital Flexible Ureteroscope (7.5F)

EUDAMED

Class IIa (EU MDR)

Ref HUS-T102R

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-T102R EUDAMED

Identifiers

Primary DI / UDI-DI
06972498490356 EUDAMED
Basic UDI-DI
6972498490100F5 EUDAMED
Direct Marketing DI
06972498490356 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

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

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 0163b9ba-fe53-4fc3-afa2-7649868409bc 61 fields · synced Jun 19, 2026