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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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sterEOS — 3 UDI-DI variants, MDR (EOS imaging)

MD Atlas
EOS imaging

Data from EUDAMED, last updated May 19, 2026

sterEOS

3663999RWS01A5

3 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: EOS imaging

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 3663999RWS01A5
Device name: sterEOS
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: Jun 12, 2023

Manufacturer & authorised representative

Manufacturer

Name: EOS imaging
SRN: FR-MF-000000502
Country: France
Email: regulatory@eos-imaging.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01H2Q4TBEGZ4F3QNKMDP5X3E3W

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

sterEOS03663999000047
sterEOS03663999000054
sterEOS03663999000153