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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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X-rays emitting devices — 2 UDI-DI variants, MDR (Imaginalis Srl)

MD Atlas
Imaginalis Srl

Data from EUDAMED, last updated May 30, 2026

X-rays emitting devices

80553857100103K

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Imaginalis Srl

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 80553857100103K
Device name: X-rays emitting devices
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Oct 11, 2024

Manufacturer & authorised representative

Manufacturer

Name: Imaginalis Srl
SRN: IT-MF-000026523
Country: Italy
Email: s.ciappi@imaginalis.it
Phone: +39 055 0463727

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J9XK6ZR5VRSGS6NJ1X3FXFWP

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

980210100008055385710022
980110300008055385710008