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Stent Coronario - Argentina Medical Device Registration

Access comprehensive regulatory information for Stent Coronario 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 18, 2024.

This page provides complete registration details including product code (416-86), brand name (Sinus DS Stent System), 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
Stent Coronario
Argentina Medical Device Registration
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Product Information

Sinus- SuperFlex-DS, sinus-Repo-DS

Device Classification
Registration Type
Registration modification (non-agile) Class III-IV
Modificaciรณn de Registro (no รกgil) Clase III-IV
Product Code
416-86
Brand Name
Sinus DS Stent System
Product Name
Stent Coronario
Registration Information
Registration Date
June 18, 2024
Database ID
cmhaytq4e07mdekuz8kg5tz7z
Authorized Representative