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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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MAIPA Assay — 2 UDI-DI variants, IVDR (Advanced Practical Diagnostics)

MD Atlas
Advanced Practical Diagnostics

Data from EUDAMED, last updated May 23, 2026

MAIPA Assay

5430000412900006Q2

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class C

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Manufacturer: Advanced Practical Diagnostics

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Device characteristics

ReagentProfessional testingHuman tissues / cells

Identity & classification

Basic UDI-DI: 5430000412900006Q2
Device name: MAIPA Assay
Device model: 900006 and 900016
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: Feb 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: Advanced Practical Diagnostics
SRN: BE-MF-000000572
Country: Belgium
Email: Raf.Berghmans@apdia.be
Phone: +32 1 445 35 99

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J879SNT8X5H6QKCA72FP1KRE

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

MAIPA Assay05430000412124
MAIPA Assay05430000412117