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Single-use Ureteral Access Sheath

EUDAMED

Class IIa (EU MDR)

Ref UA-1235Model UA-(1025、1035、1045、1125、1135、1145、1225、1235、1245、1325、1335、1345、1425、1435、1445)

by Scivita Medical Technology Co., Ltd.

Identity

Trade Name
Single-use Ureteral Access Sheath EUDAMED
Device Name
Single-use Ureteral Access Sheath EUDAMED
Model / Reference
UA-(1025、1035、1045、1125、1135、1145、1225、1235、1245、1325、1335、1345、1425、1435、1445) EUDAMED
UA-1235 EUDAMED

Identifiers

Primary DI / UDI-DI
06971381251722 EUDAMED
Basic UDI-DI
697138125021A89 EUDAMED
Direct Marketing DI
06971381251722 EUDAMED
EMDN Code
U0601 UROLOGICAL GUIDEWIRES, HYDROPHILIC EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Belgium 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 Ureteral Access Sheath by Scivita Medical Technology Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000010305
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 169f5ba0-7da8-48bf-860c-0d60ab40dc6b 61 fields · synced Jun 18, 2026