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ALKALINE PHOSPHATASE (FAL OR ALP) - ANVISA Registration 10377390291

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 10377390291 and manufactured by KATAL BIOTECNOLOGICA INDÚSTRIA E COMÉRCIO LTDA. The registration is held by KATAL BIOTECNOLOGICA INDUSTRIA E COMERCIO 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 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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10377390291
Registration Details
ANVISA Registration Number: 10377390291
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Device Details

FAMÍLIA FOSFATASE ALCALINA
Risk Class II

Registration Details

10377390291

25351000594202566

71437917000104

Company Information

Brazil
PT: BRASIL

Dates and Status

Mar 05, 2025

VIGENTE

09/18/2025 19:00:01