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Biliary Plastic Stent

EUDAMED

Class IIa (EU MDR)

Ref AF-D07005TBModel Biliary Plastic Stent

by Alton (Shanghai) Medical Instruments Co., Ltd.

Identity

Trade Name
Biliary Plastic Stent EUDAMED
Device Name
Biliary Plastic Stent EUDAMED
Model / Reference
Biliary Plastic Stent EUDAMED
AF-D07005TB EUDAMED

Identifiers

Primary DI / UDI-DI
06942127826856 EUDAMED
Basic UDI-DI
697067138PS036JZ EUDAMED
EMDN Code
G03040301 BILIARY TUBES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Biliary Plastic Stent by Alton (Shanghai) Medical Instruments 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-000012832
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 97161b0d-3b50-4132-93f6-3f1e731826a4 61 fields · synced Oct 6, 2026