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Via Go

EUDAMED

Class I (EU MDR)

Ref 1595002Model ViaGo V24Ref 1596101

by Alber GmbH

Identity

Trade Name
VIA GO EUDAMED
Device Name
ViaGo V24 EUDAMED
Model / Reference
ViaGo V24 EUDAMED
1595002 EUDAMED
1596101 EUDAMED

Identifiers

Primary DI / UDI-DI
04046727231545 EUDAMED
04046727263980 EUDAMED
Basic UDI-DI
4046727viaGOV24EH EUDAMED
EMDN Code
Y122410 ELECTRIC PROPULSION UNIT EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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

Via Go by Alber GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Alber GmbH
EUDAMED SRN
DE-MF-000005502

Sources (2)

  • EUDAMED b1d41eda-1086-4039-ad0e-9d97cb2cf0a4 61 fields · synced Jul 26, 2026
  • EUDAMED dabb363c-45ab-4f86-84bc-519ca4954ef5 61 fields · synced May 19, 2026