Kit Cânula Spineedle NucleoCore
Lumbar decompression kit · class III · Until 06/10/2035
- Registration no.
- 81747770038
- Process no.
- 25351121613202597
- Status
- Until 06/10/2035
- Device type
- Lumbar decompression kit (Kit de descompressão lombar)
- Risk class
- III
- Registration holder
- RENOVA MEDICAL INDÚSTRIA E COMÉRCIO DE PRODUTOS MÉDICOS HOSPITALARES LTDA CNPJ 31.047.312/0001-84 · 178 registrations
- Manufacturer
- Published
- 06/10/2025
- Valid until
- 06/10/2035
- Last updated by ANVISA
- 2026-10-12
- Official record
- View on ANVISA ↗