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Voyager L

EUDAMED

Class IIb (EU MDR)

Ref VA3540-L

by Alfamed Srl

Identity

Device Name
VOYAGER L EUDAMED
Model / Reference
VA3540-L EUDAMED

Identifiers

Primary DI / UDI-DI
08056479540143 EUDAMED
Basic UDI-DI
B-08056479540143 EUDAMED
EMDN Code
K020399 DEVICES FOR SURGERY WITH RADIOFREQUENCY GENERATOR, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Italy 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Voyager L by Alfamed Srl — Class IIb — 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

Manufacturer
Alfamed Srl
EUDAMED SRN
IT-MF-000033580

Sources (1)

  • EUDAMED 499f33e7-3e8a-467e-9a2e-d917916a3d2b 61 fields · synced Jun 18, 2026