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Phacoemulsification system - Argentina Medical Device Registration

Access comprehensive regulatory information for Phacoemulsification system in the Argentina medical device market through Pure Global AI's free database. This Registration modification (non-agile) Class III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on January 22, 2024.

This page provides complete registration details including product code (1209-132), brand name (CARL ZEISS), 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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Registration modification (non-agile) Class III-IV
Phacoemulsification system
Sistema de facoemulsificaciรณn
Argentina Medical Device Registration
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Product Information

Visalis 100 incl. accessories Visalis S500 incl. accessories Visalis V500 incl. accessories Quatera 700 incl. accessories

Spanish:

Visalis 100 incl. accesorios Visalis S500 incl. accesorios Visalis V500 incl. accesorios Quatera 700 incl. accesorios

Device Classification
Registration Type
Registration modification (non-agile) Class III-IV
Modificaciรณn de Registro (no รกgil) Clase III-IV
Product Code
1209-132
Brand Name
CARL ZEISS
Product Name
Phacoemulsification system
Sistema de facoemulsificaciรณn
Registration Information
Registration Date
January 22, 2024
Database ID
cmhayu89p0mo4ekuz4npgcwqy
Authorized Representative