HELICOBACTER PYLORI - ANVISA Registration 10300390630
Access comprehensive regulatory information for HELICOBACTER PYLORI in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10300390630 and manufactured by BIOHIT OYJ. The registration is held by VYTTRA DIAGNOSTICOS S.A. with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including VEDALAB, MONOBIND, INC, 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.
Device Details
Registration Details
10300390630
25351250516201962
00904728000148
Company Information
Dates and Status
May 20, 2019
VIGENTE
09/18/2025 19:00:01
HELICOBACTER PYLORI
GASTRO TEST
JSL INDUSTRIA DE TESTES PARA DIAGNOSTICO LTDA
82146060003
Sep 15, 2025
HELICOBACTER PYLORI
Celer Finecare H. pylori Teste Quantitativo
GUANGZHOU WONDFO BIOTECH CO. LTD
80537410145
Jul 14, 2025
HELICOBACTER PYLORI
IDKยฎ Helicobacter pylori antigen ELISA
IMMUNDIAGNOSTIK AG
80464810928
Jul 14, 2025
HELICOBACTER PYLORI
RIDASCREENยฎ Helicobacter
R-BIOPHARM AG
82890930009
Apr 28, 2025
HELICOBACTER PYLORI
Teste Rรกpido de Anticorpos H. pylori
HANGZHOU AICHEK MEDICAL TECHNOLOGY CO., LTD.
81472060038
Feb 17, 2025

