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Parafleet SC 014

EUDAMED

Class IIa (EU MDR)

Ref F14-010030-150

by BrosMed Medical Co., Ltd

Identity

Trade Name
Parafleet SC 014 EUDAMED
Device Name
Polux Pro / Parafleet SC 014 PTA Balloon Dilatation Catheter EUDAMED
Model / Reference
F14-010030-150 EUDAMED

Identifiers

Primary DI / UDI-DI
06942265504241 EUDAMED
Basic UDI-DI
695848140063MF EUDAMED
EMDN Code
C010402020101 PTA BALLOON DILATATION CATHETERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands 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: Peripheral angioplasty balloon catheter, basic

Parafleet SC 014 by BrosMed Medical Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral angioplasty balloon catheter, basic.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

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

Sources (1)

  • EUDAMED f49c2a71-7054-48c9-8525-6cdbb26c1944 61 fields · synced May 23, 2026