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INTRAOCULAR POLYMER ELASTIC LENS - IRIS - Argentina Medical Device Registration

Access comprehensive regulatory information for INTRAOCULAR POLYMER ELASTIC LENS - IRIS 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 August 06, 2024.

This page provides complete registration details including product code (959-152), brand name (BENCHMARK), 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
INTRAOCULAR POLYMER ELASTIC LENS - IRIS
LENTE ELASTICA DE POLIMERO INTRAOCULAR - IRIS
Argentina Medical Device Registration
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Product Information

MIOL โ€“ IRIS

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Revรกlida de Registro I-II-III-IV
Product Code
959-152
Brand Name
BENCHMARK
REPER
Product Name
INTRAOCULAR POLYMER ELASTIC LENS - IRIS
LENTE ELASTICA DE POLIMERO INTRAOCULAR - IRIS
Registration Information
Registration Date
August 06, 2024
Database ID
cmhayu5be0kfhekuzvzqfg0k5
Authorized Representative
Name
WITH S.R.L.
MED S.R.L.