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Foldable Hydrophilic Acrylic Intraocular Lens - Argentina Medical Device Registration

Access comprehensive regulatory information for Foldable Hydrophilic Acrylic Intraocular Lens 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 July 29, 2024.

This page provides complete registration details including product code (1075-234), brand name (BIOTECH), 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
Foldable Hydrophilic Acrylic Intraocular Lens
Lente Intraocular de Acrรญlico Hidrofรญlico Plegable
Argentina Medical Device Registration
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Product Information

600 ROH, 600

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Revรกlida de Registro I-II-III-IV
Product Code
1075-234
Brand Name
BIOTECH
Product Name
Foldable Hydrophilic Acrylic Intraocular Lens
Lente Intraocular de Acrรญlico Hidrofรญlico Plegable
Registration Information
Registration Date
July 29, 2024
Database ID
cmhaytq4c07deekuzmkb6c9m2
Authorized Representative