ALKALINE PHOSPHATASE (FAL OR ALP) - ANVISA Registration 10347320351

Access comprehensive regulatory information for ALKALINE PHOSPHATASE (FAL OR ALP) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10347320351 and manufactured by HORIBA INSTRUMENTS BRASIL LTDA. The registration is held by HORIBA INSTRUMENTS BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including SIEMENS HEALTHCARE DIAGNOSTICS INC., IN VITRO DIAGNOSTICA 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.

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10347320351
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Registration Details
ANVISA Registration Number: 10347320351
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

HORIBA POINTE ALKALINE PHOSPHATASE
Risk Class II

Registration Details

10347320351

25351203044202254

01759236000179

Company Information

Brazil
PT: BRASIL

Dates and Status

Aug 18, 2022

VIGENTE

09/18/2025 19:00:01

HORIBA POINTE ALKALINE PHOSPHATASE
Risk Class II

Registration Details

10347320351

25351203044202254

01759236000179

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 18, 2022

VIGENTE

09/18/2025 19:00:01