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Dry Printing Films - Argentina Medical Device Registration

Access comprehensive regulatory information for Dry Printing Films 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 March 08, 2024.

This page provides complete registration details including product code (1073-169), brand name (FUJIFILM), 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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Argentina ANMAT Data
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Revalidation of Registration I-II-III-IV
Dry Printing Films
Pelรญculas para impresiรณn Seca
Argentina Medical Device Registration
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Product Information

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Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Revรกlida de Registro I-II-III-IV
Product Code
1073-169
Brand Name
FUJIFILM
Product Name
Dry Printing Films
Pelรญculas para impresiรณn Seca
Registration Information
Registration Date
March 08, 2024
Database ID
cmhayu4ft0ji8ekuzrc2j69le
Authorized Representative