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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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ADVATx — 1 UDI-DI variant, MDR (Advalight)

MD Atlas
Advalight

Data from EUDAMED, last updated May 31, 2026

ADVATx

57000020522A00B4

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Advalight

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 57000020522A00B4
Device name: ADVATx
Device model: 1.4
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: Advalight
SRN: DK-MF-000010334
Country: Denmark
Email: info@advalight.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KS4Y829RSK8DRV8X6DANJ88Z

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

ADVATx05700002052209