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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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MAP-AD Test Oligos — 4 UDI-DI variants, IVDR (ADmit Therapeutics)

MD Atlas
ADmit Therapeutics

Data from EUDAMED, last updated May 23, 2026

MAP-AD Test Oligos

8437026887AD001YH

4 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: ADmit Therapeutics

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 8437026887AD001YH
Device name: MAP-AD Test Oligos
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: Nov 27, 2025

Manufacturer & authorised representative

Manufacturer

Name: ADmit Therapeutics
SRN: ES-MF-000042518
Country: Spain
Email: mbarrachina@admit-therapeutics.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KB2Q9N6AT6Y4ZTPF9C1WY495

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

AD001-0108437026887018
AD001-0208437026887025
AD001-0308437026887032
AD001-0408437026887049