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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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CUREO Software — 5 UDI-DI variants, MDR (CUREosity GmbH)

MD Atlas
CUREosity GmbH

Data from EUDAMED, last updated May 23, 2026

CUREO Software

42519027CUREO_1NV

5 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: CUREosity GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42519027CUREO_1NV
Device name: CUREO Software
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 20, 2023

Manufacturer & authorised representative

Manufacturer

Name: CUREosity GmbH
SRN: DE-MF-000022049
Country: Germany
Email: eudamed@cureosity.de
Phone: +492118220466

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GQ7EG71A0T0MFHDF8JXTG5KX

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

SW-2.X.X04251902700062
SW-2.X.X04251902700079
CUREO 504251902700086
SW-052404251902700055
SW-012304251902700048