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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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iBEAM evo CT Overlay — 10 UDI-DI variants, MDR

MD Atlas
3C-Medical Intelligence GmbH

Data from EUDAMED, last updated May 23, 2026

iBEAM evo CT Overlay

04056719BUDI0000000004J2

10 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: 3C-Medical Intelligence GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 04056719BUDI0000000004J2
Device name: iBEAM evo CT Overlay
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: 3C-Medical Intelligence GmbH
SRN: DE-MF-000023763
Country: Germany
Email: info@3C-medint.com
Phone: +49819196962000

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KHX3NY2VTB6APZERHD6RYD57

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

P10105-13704056719001049
P10105-17104056719001148
P10105-16004056719001094
P10105-16904056719001131
P10105-18304056719002237
P10105-18204056719002220
P10105-18104056719001179
P10105-16504056719001117
P10105-18004056719001162
P10105-17704056719001155