MYCOBACTERIUM - ANVISA Registration 80502070075
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 80502070075 and manufactured by HAIN LIFESCIENCE GMBH. The registration is held by MOBIUS LIFE SCIENCE INDUSTRIA E COMERCIO DE PRODUTOS PARA LABORATORIOS LTDA with validity until Apr 29, 2029.
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
80502070075
25351053870201907
04645160000149
Company Information
Dates and Status
Apr 29, 2019
29/04/2029
09/18/2025 19:00:01
MYCOBACTERIUM
GenoType MTBDRsl VER 2.0
Not specified
80502070068
Oct 22, 2018
MYCOBACTERIUM
GenoType MTBDRsl VER 2.0
HAIN LIFESCIENCE GMBH
80502070068
Oct 22, 2018
MYCOBACTERIUM
GENOTYPE MTBDRplus
Not specified
80502070057
Sep 18, 2017
MYCOBACTERIUM
GENOTYPE MTBDRplus
HAIN LIFESCIENCE GMBH
80502070057
Sep 18, 2017
MYCOBACTERIUM
GenoType Mycobacterium CM VER 2.0
Not specified
80502070073
Apr 01, 2019
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