17-HYDROXYPROGESTERONE (17-OHP) - NEONATAL SCREENING - ANVISA Registration 10298910105
Access comprehensive regulatory information for 17-HYDROXYPROGESTERONE (17-OHP) - NEONATAL SCREENING in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10298910105 and manufactured by manufacturer not specified. The registration is held by REVVITY DO BRASIL LTDA with validity until Jun 23, 2035.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 4 companies making the same product including WALLAC OY, LABSYSTEMS DIAGNOSTICS OY, 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
10298910105
25351219537201054
00351210000124
Company Information
Dates and Status
Jun 23, 2010
23/06/2035
09/18/2025 19:00:01
17-HIDROXIPROGESTERONA (17-OHP) - TRIAGEM NEONATAL
Neonatal 17-OH-Progesterone FEIA
LABSYSTEMS DIAGNOSTICS OY
81541770004
Aug 11, 2025
17-HIDROXIPROGESTERONA (17-OHP) - TRIAGEM NEONATAL
Neonatal 17-OH-Progesterone FEIA
Not specified
81541770004
Aug 11, 2025
17-HIDROXIPROGESTERONA (17-OHP) - TRIAGEM NEONATAL
17 alfa-OH Progesterona Test System โ ELISA
MONOBIND, INC
80048490105
May 12, 2025
17-HIDROXIPROGESTERONA (17-OHP) - TRIAGEM NEONATAL
17 alfa-OH Progesterona Test System โ ELISA
Not specified
80048490105
May 12, 2025
17-HIDROXIPROGESTERONA (17-OHP) - TRIAGEM NEONATAL
IMUNOSCREEN NEO 17-OHP DBS
MBIOLOG DIAGNOSTICOS LTDA
80047580220
Feb 14, 2024

