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Humidification chambers - Argentina Medical Device Registration

Access comprehensive regulatory information for Humidification chambers in the Argentina medical device market through Pure Global AI's free database. This Class I-II Registration medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on July 18, 2024.

This page provides complete registration details including product code (1601-140), brand name (Dräger), 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
Humidification chambers
Cámaras de humidificación
Argentina Medical Device Registration
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Product Information

MP00234; Disp. humi.chamber f.F&P MR850

Device Classification
Registration Type
Class I-II Registration
Registro Clase I-II
Product Code
1601-140
Brand Name
Dräger
Product Name
Humidification chambers
Cámaras de humidificación
Registration Information
Registration Date
July 18, 2024
Database ID
cmhayu5bc0k7hekuz21rrhu99
Authorized Representative