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Composite restaurativo de fotocurado - Argentina Medical Device Registration

Access comprehensive regulatory information for Composite restaurativo de fotocurado in the Argentina medical device market through Pure Global AI's free database. This Revalidation of Registration I-II-III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on December 14, 2022.

This page provides complete registration details including product code (510-239), brand name (Klepp), authorized representative information, registration type, and regulatory compliance data from the official Argentina ANMAT medical device database. Pure Global AI offers free access to Argentina's medical device registry, helping global MedTech companies navigate Argentina regulations efficiently.

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Revalidation of Registration I-II-III-IV
Composite restaurativo de fotocurado
Argentina Medical Device Registration
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Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Revรกlida de Registro I-II-III-IV
Product Code
510-239
Brand Name
Klepp
Product Name
Composite restaurativo de fotocurado
Registration Information
Registration Date
December 14, 2022
Database ID
cmhayua9c0o2jekuzuo7i35k6
Authorized Representative