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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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Aerolet — 28 UDI-DI variants, MDR (Aerolet - Economic Holland B.V.)

MD Atlas
Aerolet - Economic Holland B.V.

Data from EUDAMED, last updated May 30, 2026

Aerolet

87193276956AEROLET19985M

28 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: Aerolet - Economic Holland B.V.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 87193276956AEROLET19985M
Device name: Aerolet
Device model: Toilet lift
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 16, 2022

Manufacturer & authorised representative

Manufacturer

Name: Aerolet - Economic Holland B.V.
SRN: NL-MF-000010807
Country: Netherlands
Email: info@aerolet.nl
Phone: +31 533033024

Variants by status

UDI-DI variants

28 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G4DMF5YX31VSV3MGKVZSCVQR

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

Aerolet08719327695708
Aerolet08720299854536
Aerolet08720299854567

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