MYCOBACTERIUM - ANVISA Registration 10350840470

Access comprehensive regulatory information for MYCOBACTERIUM in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10350840470 and manufactured by BODITECH MED INC.. The registration is held by BIOSYS LTDA with validity until Feb 24, 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 HAIN LIFESCIENCE GMBH, BECTON DICKINSON AND COMPANY (SPARKS), 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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10350840470
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Registration Details
ANVISA Registration Number: 10350840470
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

ichroma™ IGRA-TB Tube
Risk Class III

Registration Details

10350840470

25351367127202432

02220795000179

Company Information

BODITECH MED INC.
South Korea
PT: CORÉIA DO SUL

Dates and Status

Feb 24, 2025

24/02/2035

09/18/2025 19:00:01

ichroma™ IGRA-TB Tube
Risk Class III

Registration Details

10350840470

25351367127202432

02220795000179

Company Information

Dates and Status

Feb 24, 2025

24/02/2035

09/18/2025 19:00:01