FLEXPRO PENMATE
Needle phobia device · class I · Valid
- Registration no.
- 82113060001
- Process no.
- 25351205038202401
- Status
- Valid
- Device type
- Needle phobia device (Dispositivo Para Fobia de Agulha)
- Risk class
- I
- Registration holder
- NOVO NORDISK FARMACÊUTICA DO BRASIL LTDA CNPJ 82.277.955/0007-40 · 9 registrations
- Manufacturer
- Published
- 06/05/2024
- Valid until
- No expiry (VIGENTE)
- Last updated by ANVISA
- 2026-10-12
- Official record
- View on ANVISA ↗
Other needle phobia device registrations (2 in total, see all)
| Product | Class | Holder | Published | Status |
|---|---|---|---|---|
| biovibra biomedical
10196329004 |
I | BIOMEDICAL EQUIPAMENTOS E PRODUTOS MÉDICO-CIRÚRGICOS LTDA. | 13/02/2017 | Valid |