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Prodonto Strip Abrasiva - EUDAMED Registration +E299PROCT0001F0

Access comprehensive regulatory information for Prodonto Strip Abrasiva in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI +E299PROCT0001F0 and manufactured by Polydentia SA in Switzerland.

This page provides complete registration details including trade name (Prodonto Strip abrasiva), manufacturer information, authorized representative details, 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 I
+E299PROCT0001F0
No
Prodonto Strip Abrasiva
Trade Name: Prodonto Strip abrasiva
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Device Description (EMDN)

DENTAL ABRASIVE AND POLISHING MATERIALS

Device Classification
Risk Class
Class I
CND Nomenclatures Code
Q01010403
Trade Name
Prodonto Strip abrasiva
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
+E299PROCT0001F0
Basic UDI
++E299ASTIDENTALABRASIVUE
Version Date
January 09, 2025
Manufacturer Last Update
November 08, 2024
Active Status
No
Manufacturer
Manufacturer Name
Polydentia SA
Country
Switzerland
Country Type
NON_EU
Address
47 Via Cantonale Mezzovico-Vira
Email
info@polydentia.ch
Authorized Representative
SRN
LI-AR-000008367
Country
Liechtenstein
Address
44 Heiligkreuz Vaduz
Email
quality@idd.dental
Telephone
+423 220 21 35
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
Austria:None~None, Croatia:None~None, France:None~None, Germany:None~None, Italy:None~None, Liechtenstein:None~None, Portugal:None~None, Slovenia:None~None, Spain:None~None
Device Characteristics
Human Tissues
No
Animal Tissues
No