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Interface for spontaneous ventilation - Argentina Medical Device Registration

Access comprehensive regulatory information for Interface for spontaneous ventilation in the Argentina medical device market through Pure Global AI's free database. This Revalidation of Registration I-II-III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on May 31, 2023.

This page provides complete registration details including product code (1608-61), brand name (Fisher and Paykel), 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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Revalidation of Registration I-II-III-IV
Interface for spontaneous ventilation
Interfase para ventilaciรณn espontรกnea
Argentina Medical Device Registration
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Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Revรกlida de Registro I-II-III-IV
Product Code
1608-61
Brand Name
Fisher and Paykel
Product Name
Interface for spontaneous ventilation
Interfase para ventilaciรณn espontรกnea
Registration Information
Registration Date
May 31, 2023
Database ID
cmhaytp5v06wnekuz1i20nk35
Authorized Representative