ANVISA registration

ORLIGHT KIT CÂNULA PLDD

Registration 80179630008. Kit de descompressão lombar

Registration details

Registration number80179630008
Application number25351955992201687
Technical nameKit de descompressão lombar
Risk classIII
Published on26/12/2016
ValidityValid until 26/12/2026

Registration holder

Legal nameHIGHLAS DO BRASIL LTDA
CNPJ05.208.227/0001-40

Manufacturer

  • MEGABAY S.A ARGENTINA

Other registrations held by HIGHLAS DO BRASIL LTDAview all

FIBRA ENDOLUMINAL ORLIGHT FIBER

80179630004

LASER DE TRATAMENTOS CIRÚRGICOS E TRANSDÉRMICOS

80179630006

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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