Argentina flag908-213

Reagent for quantitative determination of galactose 1 phosphate uridyltransferase in neonates

Reactivo para determinación cuantitativa de galactosa 1 fosfato uridiltransferasa en neonatos

Argentina Medical Device Registration · SPOTCHECK · CROMOION Ltd. · Registered September 27, 2023

Registration of products for IVD diagnostics - Group C and D
Device classification
Registration Type
Registration of products for IVD diagnostics - Group C and D
Registro De Productos Para Diagnóstico IVD - Grupo C Y D
Product Code
908-213
Brand Name
SPOTCHECK
Product Name
Reagent for quantitative determination of galactose 1 phosphate uridyltransferase in neonates
Reactivo para determinación cuantitativa de galactosa 1 fosfato uridiltransferasa en neonatos
Registration information
Registration Date
September 27, 2023
Database ID
cmhayu26j0ho8ekuzbxqlss10
Authorized representative
Name
CROMOION Ltd.
CROMOION SRL.
Documents
Product information

SPOTCHECK GALT MICROPLATE REAGENT KIT

About this record

Access comprehensive regulatory information for Reagent for quantitative determination of galactose 1 phosphate uridyltransferase 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 September 27, 2023.

This page provides complete registration details including product code (908-213), 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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