908-220Reagent for quantitative determination of 17-alpha-hydroxyprogesterone in neonates
Argentina Medical Device Registration · SPOTCHECK · CROMOION Ltd. · Registered July 18, 2023
Registration of products for IVD diagnostics - Group C and D- Registration Type
- Registration of products for IVD diagnostics - Group C and D
- Registro De Productos Para Diagnóstico IVD - Grupo C Y D
- Product Code
- 908-220
- Brand Name
- SPOTCHECK
- Product Name
- Reagent for quantitative determination of 17-alpha-hydroxyprogesterone in neonates
- Reactivo para determinación cuantitativa de 17 alfa-hidroxiprogesterona en neonatos
- Registration Date
- July 18, 2023
- Database ID
- cmhayu4fw0jscekuzc5dt7iiv
SPOTCHECK® 17-OHP Neonatal Screening Kit
Access comprehensive regulatory information for Reagent for quantitative determination of 17-alpha-hydroxyprogesterone in neonates in the Argentina medical device market through Pure Global AI's free database. This Registration of products for IVD diagnostics - Group C and D medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on July 18, 2023.
This page provides complete registration details including product code (908-220), brand name (SPOTCHECK), 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.