BIOTINIDASE - NEONATAL SCREENING - ANVISA Registration 10298910122

Access comprehensive regulatory information for BIOTINIDASE - NEONATAL SCREENING in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10298910122 and manufactured by WALLAC OY. The registration is held by REVVITY DO BRASIL LTDA with validity until Mar 31, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 2 companies making the same product including INTERNACIONAL CIENTÍFICA LTDA, WALLAC OY, and 4 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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Registration Details
ANVISA Registration Number: 10298910122
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

GSP NEONATAL BIOTINIDASE KIT
Risk Class III

Registration Details

10298910122

25351046637201424

00351210000124

Company Information

WALLAC OY
Finland
PT: FINLÂNDIA

Dates and Status

Mar 31, 2014

31/03/2034

09/18/2025 19:00:01

GSP NEONATAL BIOTINIDASE KIT
Risk Class III

Registration Details

10298910122

25351046637201424

00351210000124

Company Information

Dates and Status

Mar 31, 2014

31/03/2034

09/18/2025 19:00:01

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