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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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Methinks Stroke Suite — 2 UDI-DI variants, MDR (Methinks Software SL)

MD Atlas
Methinks Software SL

Data from EUDAMED, last updated May 23, 2026

Methinks Stroke Suite

8437023475MSSEUBH

2 UDI-DI variants

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

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

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8437023475MSSEUBH
Device name: Methinks Stroke Suite
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jul 13, 2023

Manufacturer & authorised representative

Manufacturer

Name: Methinks Software SL
SRN: ES-MF-000023690
Country: Spain
Email: info@methinks.es

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01H4K489NDV6G2T8V2C9DTSD1A

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

N/A08437023475027
Methinks Stroke Suite08437023475010