17-HYDROXYPROGESTERONE (17-OHP) - ANVISA Registration 80103990074
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 80103990074 and manufactured by RADIM SPA. The registration is held by RADIM LATINO AMERICA DIAGNOSTICO 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
80103990074
25351065489200791
04595434000132
Company Information
Dates and Status
May 14, 2007
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)
FAMรLIA IDS-iSYS 17-OH PROGESTERONE
IDS IMMUNODIAGNOSTIC SYSTEMS LTD.
10338930317
Aug 05, 2024
17-HIDROXIPROGESTERONA (17-OHP)
FAMรLIA KIT DE DETECรรO PARA 17a-HIDROXIPROGESTERONA (17-a-OHP) - DIRUI
DIRUI INDUSTRIAL CO. LTD
82378830060
Feb 14, 2024
17-HIDROXIPROGESTERONA (17-OHP)
Famรญlia AutoLumo 17a-OHP Micropartรญculas (CLIA)
AUTOBIO DIAGNOSTICS CO., LTD
80102513186
Feb 05, 2024
17-HIDROXIPROGESTERONA (17-OHP)
17-OH-Progesterone Saliva ELISA Free
LDN- LABOR DIAGNOSTIKA NORD GMBH & CO, KG
80464810853
Oct 02, 2023

