GASTRIN RELEASING PEPTIDE - ANVISA Registration 80102513397
Access comprehensive regulatory information for GASTRIN RELEASING PEPTIDE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80102513397 and manufactured by AUTOBIO DIAGNOSTICS CO., LTD. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Apr 07, 2035.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 3 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.
Related Devices (2)
Registration Details
80102513397
25351449737202453
04718143000194
Company Information
Dates and Status
Apr 07, 2025
07/04/2035
09/18/2025 19:00:01
PEPTÍDEO DE LIBERAÇÃO DE GASTRINA
Família ARCHITECT ProGRP
ABBOTT GMBH
80146502407
Jun 09, 2025
PEPTÍDEO DE LIBERAÇÃO DE GASTRINA
Família ARCHITECT ProGRP
Not specified
80146502407
Jun 09, 2025
PEPTÍDEO DE LIBERAÇÃO DE GASTRINA
Família MAGLUMI ProGRP (CLIA)
SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.
80102513362
Jan 27, 2025
PEPTÍDEO DE LIBERAÇÃO DE GASTRINA
Família MAGLUMI ProGRP (CLIA)
Not specified
80102513362
Jan 27, 2025
PEPTÍDEO DE LIBERAÇÃO DE GASTRINA
ProGRP Reagent Kit
LABTEST DIAGNOSTICA S/A
10009010393
May 29, 2023

