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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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GAMMA Dental Software for Windows — 5 UDI-DI variants, MDR

MD Atlas
"Gamma" Medizinisch-wissenschaftliche Fortbildungs GmbH

Data from EUDAMED, last updated May 23, 2026

GAMMA Dental Software for Windows

912012191GDSW1Z2

5 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: "Gamma" Medizinisch-wissenschaftliche Fortbildungs GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 912012191GDSW1Z2
Device name: GAMMA Dental Software for Windows
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
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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basicUdiUlid01GRNNKT0CCPMQS15G6MNWG1DD

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

03-SOFTD000AM09120121910154
03-SOFTD000AM09120121910161
03-SOFTD000AM09120121910208
GAMMA Dental Software®, "AM" Version 8.809120121910222
03-GDSWAM09120121910314