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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 June 07, 2024.

This page provides complete registration details including product code (1209-132), brand name (ZEISS MEDICEL), 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 facoemulsificación
Argentina Medical Device Registration
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Product Information

Manufacturer Carl Zeiss Meditec AG: Visalis 100 incl. accessories Visalis S500 incl. accessories Visalis V500 incl. accessories Quatera 700 incl. accessories Manufacturer Medicel AG: SMS355P Swiss l/A coaxial system at 45° angle / 21G SMS390S Swiss coaxial I/A system soft tip, 45°/ 21G angle 3032-23 Irrigation Handpiece 23G Swiss Two-Hand System L/A

Spanish:

Fabricante Carl Zeiss Meditec AG: Visalis 100 incl. accesorios Visalis S500 incl. accesorios Visalis V500 incl. accesorios Quatera 700 incl. accesorios Fabricante Medicel AG: SMS355P Sistema coaxial l/A suizo en ángulo de 45° / 21G SMS390S Sistema coaxial I/A suizo punta blanda, ángulo de 45°/ 21G 3032-23 Pieza de mano de irrigación 23G sistema bimanual l/A suizo

Device Classification
Registration Type
Registration modification (non-agile) Class III-IV
Modificación de Registro (no ágil) Clase III-IV
Product Code
1209-132
Brand Name
ZEISS MEDICEL
Product Name
Phacoemulsification system
Sistema de facoemulsificación
Registration Information
Registration Date
June 07, 2024
Database ID
cmhaytq4f07plekuz49k2usg7
Authorized Representative