Miso Ideal Ceramic Bracket
- Risk class
- Class IIa
- CND nomenclatures code
- Q010403
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 08800022215961
- Basic UDI
- 880002220MisoIdealWF
- Version date
- April 11, 2023
- Manufacturer last update
- April 14, 2022
- Active status
- No
- Manufacturer name
- HT Co., Ltd.
- Country
- Republic of Korea
- Country type
- NON_EU
- Address
- 10, Sinjeong-ro 159beon-gil, Giheung-gu Yongin-si, Gyeonggi-do
- htdental@htdental.co
- Name
- JaviTech e.K.
- SRN
- DE-AR-000005875
- Country
- Germany
- Address
- 16 Sachsenhausener Str. Schwalbach am Taunus
- info@javitech.de
- Telephone
- +49 176 7298 9240
- Competent authority
- DE/CA29 - Regierungspräsidium Darmstadt Abteilung Arbeitsschutz und Umwelt
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Germany
- Market available
- Austria:None~None, Belgium:None~None, Bulgaria:None~None, Croatia:None~None, Cyprus:None~None, Czechia:None~None, Denmark:None~None, Estonia:None~None, Finland:None~None, France:None~None, Germany:None~None, Greece:None~None, Hungary:None~None, Iceland:None~None, Ireland:None~None, Italy:None~None, Latvia:None~None, Liechtenstein:None~None, Lithuania:None~None, Luxembourg:None~None, Malta:None~None, Netherlands:None~None, Norway:None~None, Poland:None~None, Portugal:None~None, Romania:None~None, Slovakia:None~None, Slovenia:None~None, Spain:None~None, Sweden:None~None, Turkey:None~None, United Kingdom (Northern Ireland only):None~None
- Human tissues
- No
- Animal tissues
- No
ORTHODONTIC BRACKETS AND BUTTONS
Access comprehensive regulatory information for Miso Ideal Ceramic Bracket in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI 08800022215961 and manufactured by HT Co., Ltd. in Republic of Korea.
This page provides complete registration details including manufacturer information, authorized representative details, competent authority (DE/CA29 - Regierungspräsidium Darmstadt Abteilung Arbeitsschutz und Umwelt), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.