Podologie Schleifer - EUDAMED Registration E3128601040101
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 E3128601040101 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.
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EUDAMED Official Data
Class IIa
E3128601040101
No
Podologie Schleifer
Trade Name: Diamant HP
Device Description (EMDN)
ODONTOSTOMATOLOGY BURS, REUSABLE
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
E3128601040101
Basic UDI
++E31217761EX
Version Date
November 13, 2023
Manufacturer Last Update
August 20, 2021
Active Status
No
Manufacturer
Manufacturer Name
Edenta EtablissementCountry
Liechtenstein
Country Type
EU_EXTENDED
Address
13 Industriestrasse Schaanwald
Email
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