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VygoPlex Echo

EUDAMED

Class IIa (EU MDR)

Ref AEYMNVF22080

by M.D.L. S.r.l.

Identity

Trade Name
VygoPlex Echo EUDAMED
Device Name
VygoPlex Echo EUDAMED
Model / Reference
AEYMNVF22080 EUDAMED

Identifiers

Primary DI / UDI-DI
08055271572031 EUDAMED
Basic UDI-DI
B-08055271572031 EUDAMED
EMDN Code
A010302 PLEXUS BLOCK NEEDLES AND KITS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria 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

VygoPlex Echo by M.d.l. S.r.l. — Class IIa — CE/MDR — 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
M.D.L. S.r.l.
EUDAMED SRN
IT-MF-000011599

Sources (1)

  • EUDAMED a47a3b89-b85c-40f8-aff2-1e6e67eac65a 61 fields · synced Oct 7, 2026