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LIQUIFORM UV PHOSPHORUS - Argentina Medical Device Registration

Access comprehensive regulatory information for LIQUIFORM UV PHOSPHORUS in the Argentina medical device market through Pure Global AI's free database. This IVD Registration Group A and B medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on June 25, 2024.

This page provides complete registration details including product code (95-312), brand name (LIQUIFORM UV PHOSPHORUS), 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
Bilingual (Spanish/English)
IVD Registration Group A and B
LIQUIFORM UV PHOSPHORUS
FOSFORO UV LIQUIFORM
Argentina Medical Device Registration
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Product Information

PHOSPHORUS UV LIQUIFORM (Phosphorus/ Inorganic phosphate)

Spanish:

FOSFORO UV LIQUIFORM (Fรณsforo/ Fosfato inorgรกnico)

Device Classification
Registration Type
IVD Registration Group A and B
Registro IVD Grupo A y B
Product Code
95-312
Brand Name
LIQUIFORM UV PHOSPHORUS
FOSFORO UV LIQUIFORM
Product Name
LIQUIFORM UV PHOSPHORUS
FOSFORO UV LIQUIFORM
Registration Information
Registration Date
June 25, 2024
Database ID
cmhaytq4e07laekuz43t9uzb3
Authorized Representative