Kit Cânula Endoscect Plus Marden +
Lumbar decompression kit · class III · Until 24/02/2035
- Registration no.
- 82209520026
- Process no.
- 25351456370202424
- Status
- Until 24/02/2035
- Device type
- Lumbar decompression kit (Kit de descompressão lombar)
- Risk class
- III
- Registration holder
- MARDEN MEDICAL LTDA CNPJ 40.220.751/0001-38 · 509 registrations
- Manufacturer
- Published
- 24/02/2025
- Valid until
- 24/02/2035
- Last updated by ANVISA
- 2026-10-12
- Official record
- View on ANVISA ↗