PEPSINOGEN I - ANVISA Registration 10300390625
Access comprehensive regulatory information for PEPSINOGEN I in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10300390625 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 ABBOTT GMBH, LABTEST DIAGNOSTICA S/A, 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
10300390625
25351250552201926
00904728000148
Company Information
Dates and Status
May 20, 2019
VIGENTE
09/18/2025 19:00:01
PEPSINOGÊNIO I
Família AutoLumo Pepsinogênio I Micropartículas (CLIA)
AUTOBIO DIAGNOSTICS CO., LTD
80102513178
Jan 15, 2024
PEPSINOGÊNIO I
KIT DE DETECÇÃO DE PEPSINOGÊNIO I (PGI) - DIRUI
DIRUI INDUSTRIAL CO. LTD
82378830033
Jan 02, 2024
PEPSINOGÊNIO I
FAMÍLIA MAGLUMI Pepsinogen I (CLIA)
SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.
81504790373
Nov 13, 2023
PEPSINOGÊNIO I
PGI Reagent Kit
LABTEST DIAGNOSTICA S/A
10009010395
May 29, 2023
PEPSINOGÊNIO I
Pepsinogen I Determination Kit
BEIJING DIAGREAT BIOTECHNOLOGIES CO., LTD.
81086830074
May 29, 2023

