E3128591040181
Podologie Schleifer
Edenta Etablissement·Class IIa·EU EUDAMED·Trade name: Diamant HPNo
Device classification
- Risk class
- Class IIa
- CND nomenclatures code
- L159007
- Trade name
- Diamant HP
- Implantable
- No
- Reusable
- No
- Measuring function
- No
Registration information
- Primary DI
- E3128591040181
- Basic UDI
- ++E31217761EX
- Version date
- November 13, 2023
- Manufacturer last update
- August 20, 2021
- Active status
- No
Manufacturer
- Manufacturer name
- Edenta Etablissement
- Country
- Liechtenstein
- Country type
- EU_EXTENDED
- Address
- 13 Industriestrasse Schaanwald
- oliver.graetz@edenta.li
Regulatory information
- Competent authority
- Office Of Public Health
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Liechtenstein
- Market available
- Liechtenstein:2023-12-01~None
Device characteristics
- Human tissues
- No
- Animal tissues
- No
Device description (EMDN)
ODONTOSTOMATOLOGY BURS, REUSABLE
About this record
Access comprehensive regulatory information for Podologie Schleifer 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 E3128591040181 and manufactured by Edenta Etablissement in Liechtenstein.
This page provides complete registration details including trade name (Diamant HP), manufacturer information, competent authority (Office Of Public Health), 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.