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Neon Nc

EUDAMED

Class III (EU MDR)

Ref BN-30015Model Kaneka PTCA Balloon Dilatation Catheters

by KANEKA Corporation

Identity

Trade Name
NEON NC EUDAMED
Device Name
NEON NC EUDAMED
Model / Reference
Kaneka PTCA Balloon Dilatation Catheters EUDAMED
BN-30015 EUDAMED

Identifiers

Primary DI / UDI-DI
04540778148932 EUDAMED
Basic UDI-DI
B-04540778148932 EUDAMED
EMDN Code
C010401020101 PTCA BALLOON DILATION CATHETERS EUDAMED

Classification

Device Class
Class III 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

Category: Coronary angioplasty balloon catheter, cutting/scoring

Neon Nc by KANEKA Corporation — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Coronary angioplasty balloon catheter, cutting/scoring.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
KANEKA Corporation
EUDAMED SRN
JP-MF-000022143
Authorised Representative
Kaneka Medical Europe N.V. BE-AR-000010091

Sources (1)

  • EUDAMED 90ead0db-ecd1-495b-a1df-4e17e7b47807 61 fields · synced Jun 18, 2026