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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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DICOM Camera Pro — 2 UDI-DI variants, MDR (meso international GmbH)

MD Atlas
meso international GmbH

Data from EUDAMED, last updated May 23, 2026

DICOM Camera Pro

426033676-DC-Y4

2 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: meso international GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426033676-DC-Y4
Device name: DICOM Camera Pro
Device model: DC-CPB
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 17, 2022

Manufacturer & authorised representative

Manufacturer

Name: meso international GmbH
SRN: DE-MF-000006355
Country: Germany
Email: info@meso.biz
Phone: +49 3727 9697 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G86BJ2B3SMNE4THYSEDY2NKC

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

DC-CC04260336763017
DC-CPB04260336763000