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HPV Direct Chip Kit - Argentina Medical Device Registration

Access comprehensive regulatory information for HPV Direct Chip Kit in the Argentina medical device market through Pure Global AI's free database. This Agile modification of product registration 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 January 15, 2024.

This page provides complete registration details including product code (626-8492), brand name (Vitro), 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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Agile modification of product registration for IVD diagnostics - Group C and D
HPV Direct Chip Kit
Argentina Medical Device Registration
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Device Classification
Registration Type
Agile modification of product registration for IVD diagnostics - Group C and D
Modificaciรณn รgil De Registro De Productos Para Diagnรณstico IVD - Grupo C Y D
Product Code
626-8492
Brand Name
Vitro
Product Name
HPV Direct Chip Kit
Registration Information
Registration Date
January 15, 2024
Database ID
cmhayu89p0mq2ekuzsmiplgoy
Authorized Representative