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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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dicomPACS®DX-R — 2 UDI-DI variants, MDR (Oehm und Rehbein GmbH)

MD Atlas
Oehm und Rehbein GmbH

Data from EUDAMED, last updated May 23, 2026

dicomPACS®DX-R

42508029SW1000AP

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: Oehm und Rehbein GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42508029SW1000AP
Device name: dicomPACS®DX-R
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Apr 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: Oehm und Rehbein GmbH
SRN: DE-MF-000004977
Country: Germany
Email: qualitymanagement@oehm-rehbein.de
Phone: 038136600500

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01J3DB3A58ZSPC51BB4DDYQDYB

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

dicomPACS®DX-R04250802900206
dicomPACS®DX-R04250802900015