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Intraocular lens inserters - Argentina Medical Device Registration

Access comprehensive regulatory information for Intraocular lens inserters 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 January 29, 2024.

This page provides complete registration details including product code (1898-71), brand name (Action Medical), 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
Intraocular lens inserters
Insertadores de lentes intraoculares
Argentina Medical Device Registration
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Product Information

Hydrofold (IM50185 catalog), accessories: IM50184 Regular size Hydrofold cartridge, IM50184S small size Hydrofold cartridge, IM50184M MINI size Hydrofold cartridge.

Spanish:

Hydrofold (catalogo IM50185), accesorios: IM50184 Cartucho Hydrofold tamaño regular, IM50184S Cartucho Hydrofold tamaño pequeño, IM50184M Cartucho Hydrofold tamaño MINI.

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Reválida de Registro I-II-III-IV
Product Code
1898-71
Brand Name
Action Medical
Product Name
Intraocular lens inserters
Insertadores de lentes intraoculares
Registration Information
Registration Date
January 29, 2024
Database ID
cmhaytt5i09azekuzzyxohwj5
Documents
Authorized Representative