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FACE MASKS - Argentina Medical Device Registration

Access comprehensive regulatory information for FACE MASKS 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 July 29, 2024.

This page provides complete registration details including product code (1084-112), brand name (RESMED), 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
FACE MASKS
M脕SCARAS FACIALES
Argentina Medical Device Registration
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Product Information

AcuCare F1-0 AcuCare F1-1 AcuCare F1-4 AirFit, AirFit for her AirFit F10, AirFit F10 for her AirFit F20, AirFit F20 for her AirMini F20 Setup Pack AirFit F30 AirTouch F20, AirTouch F20 for her FFM hospitalario Mirage (Liberty) Mirage Quattro Mirage (Swift, Swift II) M谩scara facial completa sin ventilaci贸n (Quattro FX, Quattro Air) M谩scara facial completa sin ventilaci贸n (Mirage, Ultra Mirage) Quattro (FX, FX For Her, Air, Air for her)

Device Classification
Registration Type
Class I-II Registration Modification
Modificaci贸n de Registro Clase I-II
Product Code
1084-112
Brand Name
RESMED
Product Name
FACE MASKS
M脕SCARAS FACIALES
Registration Information
Registration Date
July 29, 2024
Database ID
cmhayu5bf0kj9ekuzseenzhdn
Authorized Representative