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Artimes

EUDAMED

Class III (EU MDR)

Ref 801-4012

by BrosMed Medical Co., Ltd

Identity

Trade Name
Artimes EUDAMED
Device Name
Artimes Balloon Dilatation Catheters EUDAMED
Model / Reference
801-4012 EUDAMED

Identifiers

Primary DI / UDI-DI
06958481426434 EUDAMED
Basic UDI-DI
B-06958481426434 EUDAMED
EMDN Code
C010401020101 PTCA BALLOON DILATION CATHETERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Coronary angioplasty balloon catheter, cutting/scoring

Artimes by BrosMed Medical Co., Ltd. — Class III — CE/MDR — 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

EUDAMED SRN
CN-MF-000007501
Authorised Representative
Brosmed Medical B.V. NL-AR-000002616

Sources (1)

  • EUDAMED 5b7f3281-af3c-4010-9796-05cda155923d 61 fields · synced Oct 8, 2026