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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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Triage24 — 1 UDI-DI variant, MDR (Platform24 Healthcare AB)

MD Atlas
Platform24 Healthcare AB

Data from EUDAMED, last updated May 31, 2026

Triage24

735012722P24001LR

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: Platform24 Healthcare AB

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Device characteristics

Active device

Legacy certificates

Certificate number: 28620125298-02
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: Intertek Medical Notified Body AB (2862)
Validity: Apr 11, 2025 → Jun 27, 2027

Identity & classification

Basic UDI-DI: 735012722P24001LR
Device name: Triage24
Device model: Triage24
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: Apr 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: Platform24 Healthcare AB
SRN: SE-MF-000026278
Country: Sweden
Email: sander.riedberg@platform24.com
Phone: +46(0)700840349‬

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01JQREZMCBGMQXSM4QSNSNW6TB

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

Triage2407350127221004