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Extension systems - Argentina Medical Device Registration

Access comprehensive regulatory information for Extension systems in the Argentina medical device market through Pure Global AI's free database. This Class I-II Registration Modification medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on June 24, 2024.

This page provides complete registration details including product code (634-274), brand name (BD™), 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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Class I-II Registration Modification
Extension systems
Sistemas de extensión
Argentina Medical Device Registration
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Product Information

G30402M Extension System with Alaris™ CC Syringe Pump, Asena™ CC Syringe Pump and IVAC™ 701/711/770/P7000 Pumps (Manufacturer 1 & 2) G30653V Lightfast extension system. Alaris™ CC Syringe Pump, Asena™ Syringe Pump, IVAC™ P7000 Pumps (Manufacturer 1 & 2)

Spanish:

G30402M Sistema de extensión con bomba de jeringa Alaris™ CC, bomba de jeringa Asena™ CC y bombas IVAC™ 701/711/770/P7000 (Fabricante 1 y 2) G30653V Sistema de extensión resistente a la luz. Bomba de jeringa Alaris™ CC, bomba de jeringa Asena™, bombas IVAC™ P7000 (Fabricante 1 y 2)

Device Classification
Registration Type
Class I-II Registration Modification
Modificación de Registro Clase I-II
Product Code
634-274
Brand Name
BD™
Product Name
Extension systems
Sistemas de extensión
Registration Information
Registration Date
June 24, 2024
Database ID
cmhayu5bh0kqpekuzta4ah9na
Authorized Representative