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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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imagiQ3 Legacy — 3 UDI-DI variants, MDR (Stille AB)

MD Atlas
Stille AB

Data from EUDAMED, last updated May 31, 2026

imagiQ3 Legacy

73323390320NM

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Stille AB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 73323390320NM
Device name: imagiQ3 Legacy
Device model: 550-1700, 550-1702, 550-1703
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 20, 2025

Manufacturer & authorised representative

Manufacturer

Name: Stille AB
SRN: SE-MF-000001228
Country: Sweden
Email: katalin.daroczy@stille.se
Phone: +46 72 402 34 14

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JPS9J2DRPA8FFTJS5SNM714Z

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

550-170307332339242480
550-170207332339242473
550-170007332339238179