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enScope™ Single Use Digital Flexible Ureteroscope

EUDAMED

Class IIa (EU MDR)

Ref U75T1S

by Ezisurg Medical Co., Ltd.

Identity

Trade Name
enScope™ Single Use Digital Flexible Ureteroscope EUDAMED
Device Name
Single Use Digital Flexible Ureteroscope EUDAMED
Model / Reference
U75T1S EUDAMED

Identifiers

Primary DI / UDI-DI
06925776131649 EUDAMED
Basic UDI-DI
69257761000901Y9 EUDAMED
EMDN Code
Z12020713 URETERORENOSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Czechia 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

enScope™ Single Use Digital Flexible Ureteroscope by Ezisurg Medical Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

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-000006742
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED e49abca3-f249-418c-8425-c1cab8c2876a 61 fields · synced Jul 14, 2026