Kit Cânula Percutaneous Endoscopy Marden
Lumbar decompression kit · class III · Until 13/07/2036
- Registration no.
- 82209529170
- Process no.
- 25351125421202398
- Status
- Until 13/07/2036
- 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
- 13/03/2023
- Valid until
- 13/07/2036
- Last updated by ANVISA
- 2026-10-12
- Official record
- View on ANVISA ↗