Pure Global

Glass ionomer dental cement - Argentina Medical Device Registration

Access comprehensive regulatory information for Glass ionomer dental cement in the Argentina medical device market through Pure Global AI's free database. This Class I-II Registration Modification medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on January 06, 2023.

This page provides complete registration details including product code (510-280), 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.

Free Database
Powered by Pure Global AI
Argentina ANMAT Data
Bilingual (Spanish/English)
Class I-II Registration Modification
Glass ionomer dental cement
Cemento dental de ionomero de vidrio
Argentina Medical Device Registration
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Information

Type I/ Glass Type I PLUS/ Glass Plus RMGIC Type II/ Glass Type II Type II LC/ Glass Type II LC Molar Type IX / Glass Molar

Device Classification
Registration Type
Class I-II Registration Modification
Modificaciรณn de Registro Clase I-II
Product Code
510-280
Brand Name
Klepp
Product Name
Glass ionomer dental cement
Cemento dental de ionomero de vidrio
Registration Information
Registration Date
January 06, 2023
Database ID
cmhayu99j0nvtekuzfu48v0sk
Authorized Representative