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Reagent for determination of biotinidase in neonates - Argentina Medical Device Registration

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.

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Argentina ANMAT Data
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Registration of products for IVD diagnostics - Group C and D
Reagent for determination of biotinidase in neonates
Reactivo para determinación de biotinidasa en neonatos
Argentina Medical Device Registration
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Product Information

SPOTCHECK® Biotinidase Microplate Reagent Kit SPOTCHECK® BLOOD SPOT CONTROLS - Negative Control SPOTCHECK® BLOOD SPOT CONTROLS - Positive Control

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
908-214
Brand Name
SPOTCHECK
Product Name
Reagent for determination of biotinidase in neonates
Reactivo para determinación de biotinidasa en neonatos
Registration Information
Registration Date
August 15, 2023
Database ID
cmhaytnv904udekuzq5bh0q3u
Documents
Authorized Representative
Name
CROMOION Ltd.
CROMOION SRL.