ANVISA registration

Probe NeoV Corona Fístula

Registration 81521800004. fibra optica

Registration details

Registration number81521800004
Application number25351228563202225
Technical namefibra optica
Risk classIII
Published on18/04/2022
ValidityValid until 29/07/2029

Registration holder

Legal nameBPF MEDICAL DISTRIBUIDORA E IMPORTADORA DE PRODUTOS MEDICOS LTDA-ME
CNPJ27.622.775/0001-55

Manufacturer

  • G.N.S. NEOLASER LTD. ISRAEL

Other registrations held by BPF MEDICAL DISTRIBUIDORA E IMPORTADORA DE PRODUTOS MEDICOS LTDA-MEview all

Probe para Dissecção e Ablação NeoV

81521800000

Kit Cânula PLDD

81521800001

GERADOR DIODO LASER NEO V

81521800002

Probe NeoV Corona Hemorróidas

81521800003

Probe NeoV Corona 360

81521800005

Tubo Endotraqueal Laser

81521809001

Source: ANVISA

Source: ANVISA open data, medical device file, updated daily. The public database provides registration validity, rather than registration status: this registration may have been cancelled before its expiry date without this being shown here. Before making purchasing, import or marketing decisions, check the ANVISA search portal.

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