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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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CARE — 2 UDI-DI variants, MDR (Medgas Technik medical systems GmbH)

MD Atlas
Medgas Technik medical systems GmbH

Data from EUDAMED, last updated May 23, 2026

CARE

912012105C02CT2

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: Medgas Technik medical systems GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 912012105C02CT2
Device name: CARE
Device model: CARE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jul 6, 2023

Manufacturer & authorised representative

Manufacturer

Name: Medgas Technik medical systems GmbH
SRN: AT-MF-000006633
Country: Austria
Email: info.at@medgas-technik.com
Phone: +43 (0) 4852 66665-0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H4NJDM7YRBBXTSHF9CZP76KD

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

C02C_AP_BLK09120121050058
C02C_AP_OH09120121050089