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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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Alstringent — 2 UDI-DI variants, MDR (Alan & Co)

MD Atlas
Alan & Co

Data from EUDAMED, last updated May 23, 2026

Alstringent

542503254ALST7X

2 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: Alan & Co

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 542503254ALST7X
Device name: Alstringent
Device model: Astringent solution
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: Alan & Co
SRN: BE-MF-000000141
Country: Belgium
Email: info@alanmedical.be
Phone: +3287311059

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KAE1H2A4D02936VZ2RC0RGCH

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

Alstringent05425032540181
Polodent Astringent Solution05425032540631