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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Avento High/Low — 4 UDI-DI variants, MDR (Haelvoet NV)

MD Atlas
Haelvoet NV

Data from EUDAMED, last updated May 23, 2026

Avento High/Low

5430002080AventoF5

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Haelvoet NV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5430002080AventoF5
Device name: Avento High/Low
Device model: Avento High/Low
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 5, 2023

Manufacturer & authorised representative

Manufacturer

Name: Haelvoet NV
SRN: BE-MF-000000056
Country: Belgium
Email: info@haelvoet.com
Phone: +3251486695

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01GX8D3KBPA6HG36ZMGKGPRGGY

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Avento High/Low Duo-line with central brake05430002080413
Avento High/low Duo-line with individual brakes05430002080451
Avento High/Low Ergo-line with central brake05430002080369
Avento High/low Ergo-line with individual brakes05430002080376