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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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MEDXRAY — 2 UDI-DI variants, MDR (MED.e.Com)

MD Atlas
MED.e.Com

Data from EUDAMED, last updated May 19, 2026

MEDXRAY

3665587ACQUISITION00001YU

2 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: MED.e.Com

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Device characteristics

Active device

Legacy certificates

Certificate number: FR25/00000027
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: SGS Belgium NV (1639)
Validity: Jan 29, 2025 → Jan 20, 2030

Identity & classification

Basic UDI-DI: 3665587ACQUISITION00001YU
Device name: MEDXRAY
Device model: MEDXRAY
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: May 26, 2023

Manufacturer & authorised representative

Manufacturer

Name: MED.e.Com
SRN: FR-MF-000003036
Country: France
Email: qualite@medecom.fr
Phone: +33 2 98 46 52 48

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H16YEKBHDXQVS4HNKGGAB8GZ

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

XR.7.103665587000170
7.003665587000125