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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 Couchtop, iBEAM one Couchtop — 13 UDI-DI variants, MDR

MD Atlas
3C-Medical Intelligence GmbH

Data from EUDAMED, last updated May 23, 2026

iBEAM evo Couchtop, iBEAM one Couchtop

04056719BUDI0000000003HY

13 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: 04056719BUDI0000000003HY
Device name: iBEAM evo Couchtop, iBEAM one Couchtop
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

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KHX1FC46F5MMV98SDKT85K1B

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

P10105-12804056719001025
P10105-42604056719001926
P10105-14904056719001063
P10105-16304056719001100
P10105-18404056719002251
P10105-14804056719001056
P10105-41204056719001292
P10105-42304056719001322
P10105-41304056719001308
P10105-41404056719001315
P10105-42504056719001346
P10105-11004056719001001
P10105-30004056719002213