17-HYDROXYPROGESTERONE (17-OHP) - ANVISA Registration 80464810853
Access comprehensive regulatory information for 17-HYDROXYPROGESTERONE (17-OHP) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80464810853 and manufactured by LDN- LABOR DIAGNOSTIKA NORD GMBH & CO, KG. The registration is held by ARGOSLAB 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 DIAMETRA SRL, DRG INSTRUMENTS GMBH, 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
80464810853
25351571973202374
09377976000152
Company Information
Dates and Status
Oct 02, 2023
VIGENTE
09/18/2025 19:00:01
17-HIDROXIPROGESTERONA (17-OHP)
17-a- Hydroxyprogesterone Reagent Kit
VIRTUE DIAGNOSTICS SUZHOU CO. LTD.
10009010499
Aug 18, 2025
17-HIDROXIPROGESTERONA (17-OHP)
FAMÍLIA IDS-iSYS 17-OH PROGESTERONE
IDS IMMUNODIAGNOSTIC SYSTEMS LTD.
10338930317
Aug 05, 2024
17-HIDROXIPROGESTERONA (17-OHP)
FAMÍLIA KIT DE DETECÇÃO PARA 17a-HIDROXIPROGESTERONA (17-a-OHP) - DIRUI
DIRUI INDUSTRIAL CO. LTD
82378830060
Feb 14, 2024
17-HIDROXIPROGESTERONA (17-OHP)
Família AutoLumo 17a-OHP Micropartículas (CLIA)
AUTOBIO DIAGNOSTICS CO., LTD
80102513186
Feb 05, 2024
17-HIDROXIPROGESTERONA (17-OHP)
17-OH-Progesterona ELISA
EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA
10338930242
Dec 10, 2020

