RENIN - ANVISA Registration 81086830055
Access comprehensive regulatory information for RENIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81086830055 and manufactured by LDN- LABOR DIAGNOSTIKA NORD GMBH & CO, KG. The registration is held by FASTTEST DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA 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 LDN, SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD., 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
81086830055
25351081766202322
20037992000139
Company Information
Dates and Status
Mar 06, 2023
VIGENTE
09/18/2025 19:00:01
RENINA
KIT DE DETECÇÃO PARA RENINA - DIRUI
DIRUI INDUSTRIAL CO. LTD
82378830036
Jan 02, 2024
RENINA
Família AutoLumo Renina Micropartículas (CLIA)
AUTOBIO DIAGNOSTICS CO., LTD
80102513097
Oct 09, 2023
RENINA
Família MAGLUMI Renina Direta (CLIA)
SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.
80102513085
Sep 04, 2023
RENINA
MAGLUMI Renina Direta (CLIA)
SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.
80102512570
Sep 08, 2020
RENINA
Plasma Renin Activity (PRA)
DBC-DIAGNOSTICS BIOCHEM CANADA INC.
10300390504
May 20, 2019

