INORGANIC PHOSPHORUS/PHOSPHATE - ANVISA Registration 80657030059
Access comprehensive regulatory information for INORGANIC PHOSPHORUS/PHOSPHATE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80657030059 and manufactured by DAILYTECH LATINO AMERICA LTDA. The registration is held by DAILYTECH LATINO AMERICA LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including BIOSYSTEMS S.A., QUIBASA QUÍMICA BÁSICA LTDA, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Registration Details
80657030059
25351430519202445
03611875000118
Company Information
Dates and Status
Jan 06, 2025
VIGENTE
09/18/2025 19:00:01
FÓSFORO/FOSFATO INORGÂNICO
FAMÍLIA FÓSFORO
KATAL BIOTECNOLOGICA INDÚSTRIA E COMÉRCIO LTDA
10377390317
Jun 02, 2025
FÓSFORO/FOSFATO INORGÂNICO
KIT FÓSFORO UV
MEDMAX COMÉRCIO DE EQUIPAMENTOS MÉDICOS E SIMILARES LTDA ME
81313770062
May 26, 2025
FÓSFORO/FOSFATO INORGÂNICO
PHOPHORUS
DAILYTECH LATINO AMERICA LTDA
80657030051
Dec 23, 2024
FÓSFORO/FOSFATO INORGÂNICO
Horiba Pointe Inorganic Phosphorus
HORIBA INSTRUMENTS BRASIL LTDA
10347320379
Mar 04, 2024
FÓSFORO/FOSFATO INORGÂNICO
Horiba Pointe Inorganic Phosphorus
HORIBA INSTRUMENTS INCORPORATED
10347320379
Mar 04, 2024

