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Angiography set

EUDAMED

Class I (EU MDR)

Ref TRO040-02Model Interventional Surgical PackModel Interventional Surgical Pack

by Cobes Industries(Hefei) Co., Ltd

Identity

Trade Name
Angiography set EUDAMED
Angiography set sterile EUDAMED
Device Name
Angiography set EUDAMED
Interventional Surgical Pack EUDAMED
Model / Reference
Interventional Surgical Pack EUDAMED
TRO040-02 EUDAMED

Identifiers

Primary DI / UDI-DI
06956288671132 EUDAMED
Basic UDI-DI
B-06956288671132 EUDAMED
69562886LA0001KV EUDAMED
EMDN Code
T0202 SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Angiography set by Cobes Industries(Hefei) Co., Ltd — Class I — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000012364
Authorised Representative
DISPOMED S.A.S FR-AR-000000891

Sources (2)

  • EUDAMED 09cd5524-ba93-4a59-8de2-e299af35b443 61 fields · synced Sep 18, 2026
  • EUDAMED 1ec6cb8d-f275-4b48-bde8-8d27ae19d113 61 fields · synced May 19, 2026