← Back to catalogue

Digital Flexible Ureteroscope for Single Use

EUDAMED

Class IIa (EU MDR)

Ref XFGC-FU-670R

by Anhui Happiness Workshop Medical Instruments Co., Ltd

Identity

Trade Name
Digital Flexible Ureteroscope for Single Use EUDAMED
Device Name
Digital Flexible Ureteroscope EUDAMED
Model / Reference
XFGC-FU-670R EUDAMED

Identifiers

Primary DI / UDI-DI
06972498490011 EUDAMED
Basic UDI-DI
6972498490100F5 EUDAMED
Direct Marketing DI
06972498490011 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

Digital Flexible Ureteroscope for Single Use 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED e304309e-4055-461a-9920-d00eba1af29b 61 fields · synced Jun 20, 2026