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Avento Day-flex

EUDAMED

Class I (EU MDR)

Ref 22000

by Haelvoet NV

Identity

Trade Name
Avento Day-flex EUDAMED
Device Name
Avento Day-flex EUDAMED
Model / Reference
22000 EUDAMED

Identifiers

Primary DI / UDI-DI
05430002080499 EUDAMED
Basic UDI-DI
5430002080AventodayflexVY EUDAMED
Direct Marketing DI
05430002080499 EUDAMED
EMDN Code
V08020101 GENERIC USE ELECTRIC MEDICAL CHAIRS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium 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

Avento Day-flex by Haelvoet NV — 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
Haelvoet NV
EUDAMED SRN
BE-MF-000000056

Sources (1)

  • EUDAMED b071188e-a38c-41a4-a608-f67660ba2a63 61 fields · synced Jul 28, 2026