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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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CADIAX IV — 5 UDI-DI variants, MDR

MD Atlas
"Gamma" Medizinisch-wissenschaftliche Fortbildungs GmbH

Data from EUDAMED, last updated May 23, 2026

CADIAX IV

912012191CADIAXSW

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: "Gamma" Medizinisch-wissenschaftliche Fortbildungs GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 912012191CADIAXSW
Device name: CADIAX IV
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 7, 2023

Manufacturer & authorised representative

Manufacturer

Name: "Gamma" Medizinisch-wissenschaftliche Fortbildungs GmbH
SRN: AT-MF-000004222
Country: Austria
Email: office@gammadental.com
Phone: +43 2243 34140

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GRNT8SN5XKGZ4E2ZCST5V4X5

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

08-00G20009120121910024
08-SP025009120121910017
01-10D200-209120121910055
01-SP006509120121910048
07-10D200-209120121910031