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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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teora mind — 2 UDI-DI variants, MDR (Living Brain GmbH)

MD Atlas
Living Brain GmbH

Data from EUDAMED, last updated May 23, 2026

teora mind

PP1076900156

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Living Brain GmbH

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Device characteristics

Active device

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: PP1076900156
Device name: teora mind
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: May 25, 2023

Manufacturer & authorised representative

Manufacturer

Name: Living Brain GmbH
SRN: DE-MF-000010266
Country: Germany
Email: hello@livingbrain.de

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H19FV34982Z0WAJFA0JY9QVW

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

1.1.2.e-41/2023111682351904
2.0.0.a-43/2023111727127578