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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 Facebow kinematisch — 6 UDI-DI variants, MDR

MD Atlas
"Gamma" Medizinisch-wissenschaftliche Fortbildungs GmbH

Data from EUDAMED, last updated May 23, 2026

GAMMA Facebow kinematisch

912012191FBKINXF

6 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 912012191FBKINXF
Device name: GAMMA Facebow kinematisch
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

6 UDI-DI variants

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Applied filters

basicUdiUlid01GRP0E3P9WWYMMWXN912GNF6Y

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

Condylograph comfort I09120121910253
04-GCR311I09120121910130
Condylograph comfort I Set complete09120121910246
04-GCR00709120121910123
Condylograph Set09120121910215
Condylograph Set complete09120121910239