MYCOBACTERIUM - ANVISA Registration 10350840461

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 10350840461 and manufactured by BODITECH MED INC.. The registration is held by BIOSYS LTDA with validity until Aug 05, 2034.

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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10350840461
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Registration Details
ANVISA Registration Number: 10350840461
Janaina dos Santos de Miranda

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Related Devices (2)

Família ichroma™ IGRA-TB
Risk Class III

Registration Details

10350840461

25351033230202481

02220795000179

Company Information

BODITECH MED INC.
South Korea
PT: CORÉIA DO SUL

Dates and Status

Aug 05, 2024

05/08/2034

09/18/2025 19:00:01

Família ichroma™ IGRA-TB
Risk Class III

Registration Details

10350840461

25351033230202481

02220795000179

Company Information

Dates and Status

Aug 05, 2024

05/08/2034

09/18/2025 19:00:01