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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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Aiforia® Clinical Suite Viewer — 4 UDI-DI variants, IVDR

MD Atlas
Aiforia Technologies Plc

Data from EUDAMED, last updated May 23, 2026

Aiforia® Clinical Suite Viewer

06429810612SU001RQ

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: Aiforia Technologies Plc

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 06429810612SU001RQ
Device name: Aiforia® Clinical Suite Viewer
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Special device type: refdata.special-ivd-device-type.software
Version date: Nov 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: Aiforia Technologies Plc
SRN: FI-MF-000008986
Country: Finland
Email: contact@aiforia.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K9A7KVZZATVNQV9DCWSPCX2Z

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

Aiforia® Clinical Suite Viewer06429810612168
Aiforia® Clinical Suite Viewer06429810612182
Aiforia® Clinical Suite Viewer06429810612267
Aiforia® Clinical Suite Viewer06429810612199