1240-78HEARING FUNCTION SCREENING DEVICE
Argentina Medical Device Registration · RESONANCE · WIDEX ARGENTINA S A · Registered January 18, 2024
Class I-II Registration Modification- Registration Type
- Class I-II Registration Modification
- Modificación de Registro Clase I-II
- Product Code
- 1240-78
- Brand Name
- RESONANCE
- Product Name
- HEARING FUNCTION SCREENING DEVICE
- DISPOSITIVO PARA TAMIZAJE DE LA FUNCIÓN AUDITIVA
- Registration Date
- January 18, 2024
- Database ID
- cmhaytt5j09dpekuzem69cklk
R140 TEOAE SCREENER R140 TEOAE ADVANCED SCREENER R140 DPAOE ADVANCED SCREENER R140 TE+DPOAE ADVANCED SCREENER
Access comprehensive regulatory information for HEARING FUNCTION SCREENING DEVICE 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 January 18, 2024.
This page provides complete registration details including product code (1240-78), brand name (RESONANCE), 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.