Urinary sediment - ANVISA Registration 81778810025
Access comprehensive regulatory information for Urinary sediment in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81778810025 and manufactured by ZHUHAI KEYU BIOLOGICAL ENGINEERING CO., LTD.. The registration is held by LATIN HEALTH IMPORTADORA E DISTRIBUIDORA LTDA. with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including DIRUI INDUSTRIAL CO., LTD., DIRUI INDUSTRIAL 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
81778810025
25351808427202302
29986299000187
Company Information
Dates and Status
Jan 02, 2024
VIGENTE
09/18/2025 19:00:01
Sedimento urinário
Calibrador de Sedimento – US I
ZYBIO INC.
82533950039
Oct 09, 2023
Sedimento urinário
Controle de Sedimento I
ZYBIO INC.
82533950043
Oct 09, 2023
Sedimento urinário
FE CALIBRATOR II
DIRUI INDUSTRIAL CO. LTD.
80345000311
Jul 20, 2020
Sedimento urinário
Família FE Control II Positive Control
DIRUI INDUSTRIAL CO. LTD.
80345000308
Jun 15, 2020
Sedimento urinário
FE Control II Negative Control
DIRUI INDUSTRIAL CO. LTD.
80345000304
Mar 09, 2020

