Pure Global

Reagent for quantitative determination of TSH concentration in neonates. - Argentina Medical Device Registration

Access comprehensive regulatory information for Reagent for quantitative determination of TSH concentration 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 October 10, 2023.

This page provides complete registration details including product code (908-221), 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.

Free Database
Powered by Pure Global AI
Argentina ANMAT Data
Bilingual (Spanish/English)
Registration of products for IVD diagnostics - Group C and D
Reagent for quantitative determination of TSH concentration in neonates.
Reactivo para determinaci贸n cuantitativa de la concentraci贸n de TSH en neonatos.
Argentina Medical Device Registration
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Information

SPOTCHECK TSH NEONATAL SCREENING KIT

Device Classification
Registration Type
Registration of products for IVD diagnostics - Group C and D
Registro De Productos Para Diagn贸stico IVD - Grupo C Y D
Product Code
908-221
Brand Name
SPOTCHECK
Product Name
Reagent for quantitative determination of TSH concentration in neonates.
Reactivo para determinaci贸n cuantitativa de la concentraci贸n de TSH en neonatos.
Registration Information
Registration Date
October 10, 2023
Database ID
cmhazbf7z0dn6ekwi8xvolmlv
Documents
Authorized Representative
Name
CROMOION Ltd.
CROMOION SRL.