1608-61Interface for spontaneous ventilation
Argentina Medical Device Registration · Fisher and Paykel · DRIPLAN SOCIEDAD ANONIMA · Registered May 31, 2023
Revalidation of Registration I-II-III-IV- Registration Type
- Revalidation of Registration I-II-III-IV
- Reválida de Registro I-II-III-IV
- Product Code
- 1608-61
- Brand Name
- Fisher and Paykel
- Product Name
- Interface for spontaneous ventilation
- Interfase para ventilación espontánea
- Registration Date
- May 31, 2023
- Database ID
- cmhaytp5v06wnekuz1i20nk35
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 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.