959-152INTRAOCULAR POLYMER ELASTIC LENS - IRIS
Argentina Medical Device Registration · BENCHMARK · WITH S.R.L. · Registered August 06, 2024
Revalidation of Registration I-II-III-IV- Registration Type
- Revalidation of Registration I-II-III-IV
- Reválida 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 Date
- August 06, 2024
- Database ID
- cmhayu5be0kfhekuzvzqfg0k5
MIOL – IRIS
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.