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Vivo

EUDAMED

Class IIa (EU MDR)

Ref 100

by AURIMOD GmbH

Identity

Device Name
VIVO EUDAMED
Model / Reference
100 EUDAMED

Identifiers

Primary DI / UDI-DI
09120112971003 EUDAMED
Basic UDI-DI
B-09120112971003 EUDAMED
EMDN Code
Z12101106 NEUROLOGICAL STIMULATORS 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

Category: Point aesthesiometer

Vivo by AURIMOD GmbH — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Point aesthesiometer.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
AURIMOD GmbH
EUDAMED SRN
AT-MF-000000433

Sources (1)

  • EUDAMED d093246b-c36f-40bd-b471-a132bad58e35 61 fields · synced Jun 18, 2026