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Photopolymerizable composite for filling in posterior block - Argentina Medical Device Registration

Access comprehensive regulatory information for Photopolymerizable composite for filling in posterior block in the Argentina medical device market through Pure Global AI's free database. This Class I-II Registration medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on May 22, 2024.

This page provides complete registration details including product code (1139-214), brand name (3M ESPE), 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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Class I-II Registration
Photopolymerizable composite for filling in posterior block
Composite fotopolimerizable para relleno en bloque posterior
Argentina Medical Device Registration
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Product Information

3M Filtek One Bulk Fill Restorative : 4868A1, 4868A2. 4868A3.

Device Classification
Registration Type
Class I-II Registration
Registro Clase I-II
Product Code
1139-214
Brand Name
3M ESPE
Product Name
Photopolymerizable composite for filling in posterior block
Composite fotopolimerizable para relleno en bloque posterior
Registration Information
Registration Date
May 22, 2024
Database ID
cmhayu7b50lxbekuzuq5u6ufq
Authorized Representative