Neonatal 17-OH-Progesterone FEIA
17-Hydroxyprogesterone (17-OHP) - newborn screening · class III · Until 11/08/2035
- Registration no.
- 81541770004
- Process no.
- 25351038678202572
- Status
- Until 11/08/2035
- Device type
- 17-Hydroxyprogesterone (17-OHP) - newborn screening (17-HIDROXIPROGESTERONA (17-OHP) - TRIAGEM NEONATAL)
- Risk class
- III
- Registration holder
- SUPER DIAGNOSTICA PRODS HOSP LTDA EPP CNPJ 27.437.056/0001-64 · 4 registrations
- Manufacturer
- Published
- 11/08/2025
- Valid until
- 11/08/2035
- Last updated by ANVISA
- 2026-10-12
- Official record
- View on ANVISA ↗
Other 17-hydroxyprogesterone (17-ohp) - newborn screening registrations (5 in total, see all)
| Product | Class | Holder | Published | Status |
|---|---|---|---|---|
| 17 alfa-OH Progesterona Test System – ELISA
80048490105 |
III | USA DIAGNOSTICA LTDA | 12/05/2025 | Until 12/05/2035 |
| IMUNOSCREEN NEO 17-OHP DBS
80047580220 |
III | MBIOLOG DIAGNÓSTICOS LTDA | 14/02/2024 | Until 14/02/2034 |
| GSP Neonatal 17 a-OH-progesterone kit
10298910105 |
III | REVVITY DO BRASIL LTDA | 23/06/2010 | Until 23/06/2035 |
| KIT DELFIA AUTODELFIA 17 ALFA-HIDROXIPROGESTERONA NEONATAL
10298910015 |
III | REVVITY DO BRASIL LTDA | 23/09/1996 | Until 23/09/2036 |