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.

Janaina dos Santos de Miranda
🇧🇷 Brazil Regulatory Expert
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Contact Pure Global Brazil TeamRelated Devices (2)
Registration Details
10350840470
25351367127202432
02220795000179
Company Information
Dates and Status
Feb 24, 2025
24/02/2035
09/18/2025 19:00:01
MYCOBACTERIUM
AFIAS IGRA-TB
Not specified
10350840460
Jul 22, 2024
MYCOBACTERIUM
AFIAS IGRA-TB
BODITECH MED INC.
10350840460
Jul 22, 2024
MYCOBACTERIUM
VIDAS® TB-IGRA (TBRA)
BIOMERIEUX SA
10158120735
Oct 18, 2021
MYCOBACTERIUM
VIDAS® TB-IGRA (TBRA)
Not specified
10158120735
Oct 18, 2021
MYCOBACTERIUM
QuantiFERON®-TB GOLD Plus (QFT® Plus)
Not specified
10322250071
Sep 05, 2016
MYCOBACTERIUM
RIDA® TB Tubes
R-BIOPHARM AG
82890930018
Sep 15, 2025
MYCOBACTERIUM
RIDA® TB Tubes
Not specified
82890930018
Sep 15, 2025
MYCOBACTERIUM
RIDA®QUICK TB
Not specified
82890930015
Jul 07, 2025
MYCOBACTERIUM
RIDA®QUICK TB
R-BIOPHARM AG
82890930015
Jul 07, 2025
MYCOBACTERIUM
RIDASCREEN® TB
R-BIOPHARM AG
82890930012
Jun 23, 2025