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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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Digital Therapist — 1 UDI-DI variant, MDR (Sword Health S.A.)

MD Atlas
Sword Health S.A.

Data from EUDAMED, last updated May 31, 2026

Digital Therapist

5065013876DTC4

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Sword Health S.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5065013876DTC4
Device name: Digital Therapist
Device model: Version 2
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Mar 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: Sword Health S.A.
SRN: PT-MF-000039126
Country: Portugal
Email: regulatory@swordhealth.com
Phone: +351 223248286

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01KKEZQB0XZB4ZBEW7MFRJ0YMP

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

Digital Therapist05065013876009