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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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preOx LOR — 9 UDI-DI variants, MDR (preOx.RS GmbH)

MD Atlas
preOx.RS GmbH

Data from EUDAMED, last updated May 23, 2026

preOx LOR

42607021512151866

9 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: preOx.RS GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42607021512151866
Device name: preOx LOR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 27, 2021

Manufacturer & authorised representative

Manufacturer

Name: preOx.RS GmbH
SRN: DE-MF-000005017
Country: Germany
Email: sales@preox.de
Phone: +49 6431-21579-0

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01FK0EC311D92G72AHDJ8D00K4

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

preOx LOR04260702150434
preOx LOR04260702150052
preOx LOR04260702150427
preOx LOR04260702150038
preOx LOR04260702150014
preOx LOR04260702150069
preOx LOR04260702150007
preOx LOR04260702150045
preOx LOR04260702150021