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BioFreedom

EUDAMED

Class III (EU MDR)

Ref BFR1-3542

by Biosensors Europe SA

Identity

Device Name
BioFreedom EUDAMED
Model / Reference
BFR1-3542 EUDAMED

Identifiers

Primary DI / UDI-DI
08888893028682 EUDAMED
Basic UDI-DI
B-08888893028682 EUDAMED
EMDN Code
P070402010302 CORONARY DRUG ELUTING STENTS (DES) WITHOUT POLYMERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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

Yes

EUDAMED

BioFreedom by Biosensors Europe SA — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CH-MF-000015764
Authorised Representative
NVT GmbH DE-AR-000006441

Sources (1)

  • EUDAMED 9f6e33f3-f136-48aa-92e9-da36e26d7a5c 61 fields · synced Jun 18, 2026