BORDETELLA PERTUSSIS - ANVISA Registration 10339840415

Access comprehensive regulatory information for BORDETELLA PERTUSSIS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10339840415 and manufactured by manufacturer not specified. The registration is held by DIASORIN LTDA with validity until Aug 17, 2035.

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 DIASORIN ITALIA S.P.A., EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG, 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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10339840415
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Registration Details
ANVISA Registration Number: 10339840415
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

LIAISON Control Bordetella pertussis Toxin IgA
Risk Class III

Registration Details

10339840415

25351370522201545

01896764000170

Company Information

Dates and Status

Aug 17, 2015

17/08/2035

09/18/2025 19:00:01

LIAISON Control Bordetella pertussis Toxin IgA
Risk Class III

Registration Details

10339840415

25351370522201545

01896764000170

Company Information

Italy
PT: ITÁLIA

Dates and Status

Aug 17, 2015

17/08/2035

09/18/2025 19:00:01