Argentina flag961-62

Electrode for endocardial stimulation

Electrodo para la estimulación endocárdica

Argentina Medical Device Registration · Abbott; St. Jude Medical · ST. JUDE MEDICAL ARGENTINA S.A. · Registered January 22, 2024

Registration modification (non-agile) Class III-IV
Device classification
Registration Type
Registration modification (non-agile) Class III-IV
Modificación de Registro (no ágil) Clase III-IV
Product Code
961-62
Brand Name
Abbott; St. Jude Medical
Product Name
Electrode for endocardial stimulation
Electrodo para la estimulación endocárdica
Registration information
Registration Date
January 22, 2024
Database ID
cmhayu89p0mo3ekuzo54b95vl
Authorized representative
Documents
Product information

IsoFlex (Conditional MR) 1944-46 IsoFlex (Conditional MR) 1944-52 IsoFlex (Conditional MR) 1948-52 IsoFlex (Conditional MR) 1948-58

Spanish:

IsoFlex (MR Condicional) 1944-46 IsoFlex (MR Condicional) 1944-52 IsoFlex (MR Condicional) 1948-52 IsoFlex (MR Condicional) 1948-58

About this record

Access comprehensive regulatory information for Electrode for endocardial stimulation 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 (961-62), brand name (Abbott; St. Jude Medical), 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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