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Reagent for quantitative determination of 17-alpha-hydroxyprogesterone in neonates - Argentina Medical Device Registration

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.

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Registration of products for IVD diagnostics - Group C and D
Reagent for quantitative determination of 17-alpha-hydroxyprogesterone in neonates
Reactivo para determinaci贸n cuantitativa de 17 alfa-hidroxiprogesterona en neonatos
Argentina Medical Device Registration
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Product Information

SPOTCHECK庐 17-OHP 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
908-220
Brand Name
SPOTCHECK
Product Name
Reagent for quantitative determination of 17-alpha-hydroxyprogesterone in neonates
Reactivo para determinaci贸n cuantitativa de 17 alfa-hidroxiprogesterona en neonatos
Registration Information
Registration Date
July 18, 2023
Database ID
cmhayu4fw0jscekuzc5dt7iiv
Documents
Authorized Representative
Name
CROMOION Ltd.
CROMOION SRL.