ORLIGHT KIT CÂNULA PLDD
Lumbar decompression kit · class III · Until 26/12/2026
- Registration no.
- 80179630008
- Process no.
- 25351955992201687
- Status
- Until 26/12/2026
- Device type
- Lumbar decompression kit (Kit de descompressão lombar)
- Risk class
- III
- Registration holder
- HIGHLAS DO BRASIL LTDA CNPJ 05.208.227/0001-40 · 10 registrations
- Manufacturer
- Published
- 26/12/2016
- Valid until
- 26/12/2026
- Last updated by ANVISA
- 2026-10-12
- Official record
- View on ANVISA ↗