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Electrode for endocardial stimulation - Argentina Medical Device Registration

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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Argentina ANMAT Data
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Registration modification (non-agile) Class III-IV
Electrode for endocardial stimulation
Electrodo para la estimulaciรณn endocรกrdica
Argentina Medical Device Registration
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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

Device Classification
Registration Type
Registration modification (non-agile) Class III-IV
Modificaciรณn de Registro (no รกgil) Clase III-IV
Product Code
961-62
Brand Name
Abbott; St. Jude Medical
Product Name
Electrode for endocardial stimulation
Electrodo para la estimulaciรณn endocรกrdica
Registration Information
Registration Date
January 22, 2024
Database ID
cmhayu89p0mo3ekuzo54b95vl
Authorized Representative