1608-61Interface for spontaneous ventilation
Argentina Medical Device Registration · Fisher and Paykel · DRIPLAN SOCIEDAD ANONIMA · Registered March 17, 2023
Class I-II Registration Modification- Registration Type
- Class I-II Registration Modification
- Modificación de Registro Clase I-II
- Product Code
- 1608-61
- Brand Name
- Fisher and Paykel
- Product Name
- Interface for spontaneous ventilation
- Interfase para ventilación espontánea
- Registration Date
- March 17, 2023
- Database ID
- cmhaytu130a2yekuzqnegwv39
OPT942 OPT942E OPT944 OPT944E OPT946 OPT946E OPT970 OPT970E OPT980 OPT980E OPT962 OPT964 OPT966
Access comprehensive regulatory information for Interface for spontaneous ventilation 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 March 17, 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.