GLUTAMATE DEHYDROGENASE (GDH) IN FECES - C. DIFFICILE - ANVISA Registration 81086830102
Access comprehensive regulatory information for GLUTAMATE DEHYDROGENASE (GDH) IN FECES - C. DIFFICILE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81086830102 and manufactured by VEDALAB. The registration is held by FASTTEST DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA with validity until Mar 24, 2035.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search. 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
81086830102
25351354186202441
20037992000139
Company Information
Dates and Status
Mar 24, 2025
24/03/2035
09/18/2025 19:00:01
CLOSTRIDIUM DIFFICILE (CLOSTRIDIOIDES DIFFICILE)
FASTLINE CLOSTRIDIUM GDH
KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA
80105220181
Mar 25, 2024
CLOSTRIDIUM DIFFICILE (CLOSTRIDIOIDES DIFFICILE)
Lab Rapid GDH / Toxin A and B
LABTEST DIAGNOSTICA S/A
10009010460
Sep 16, 2024
CLOSTRIDIUM DIFFICILE (CLOSTRIDIOIDES DIFFICILE)
TRIO TOXIN A/B/GDH-CHECK-1
Not specified
81086830097
Feb 24, 2025
CLOSTRIDIUM DIFFICILE (CLOSTRIDIOIDES DIFFICILE)
TRIO TOXIN A/B/GDH-CHECK-1
VEDALAB
81086830097
Feb 24, 2025
CLOSTRIDIUM DIFFICILE (CLOSTRIDIOIDES DIFFICILE)
LIAISON C. difficile GDH
DIASORIN INC
10339840385
Jul 01, 2013