908-214Reagent for determination of biotinidase in neonates
Argentina Medical Device Registration · SPOTCHECK · CROMOION Ltd. · Registered August 15, 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
- 908-214
- Brand Name
- SPOTCHECK
- Product Name
- Reagent for determination of biotinidase in neonates
- Reactivo para determinación de biotinidasa en neonatos
- Registration Date
- August 15, 2023
- Database ID
- cmhaytnv904udekuzq5bh0q3u
SPOTCHECK® Biotinidase Microplate Reagent Kit SPOTCHECK® BLOOD SPOT CONTROLS - Negative Control SPOTCHECK® BLOOD SPOT CONTROLS - Positive Control
Access comprehensive regulatory information for Reagent for determination of biotinidase 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 August 15, 2023.
This page provides complete registration details including product code (908-214), 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.