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ANVISA registration 80195529019Active

Lumbar decompression kit

ANVISA Registration Number: 80195529019BRAMSYS INDÚSTRIA E COMÉRCIO LTDABRAMSYS INDÚSTRIA E COMÉRCIO LTDARisk Class II
Verified
Device names
Technical name
Lumbar decompression kit
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PT: Kit de descompressão lombar
Commercial name
Kit Cânula DiscGuide
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Risk class
Class II
Registration details
Registration Number
80195529019
Process Number
25351082600202676
CNPJ
04729995000187
Company information
Registration Holder
BRAMSYS INDÚSTRIA E COMÉRCIO LTDA
Manufacturer
BRAMSYS INDÚSTRIA E COMÉRCIO LTDA
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
May 25, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Lumbar decompression kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80195529019 and manufactured by BRAMSYS INDÚSTRIA E COMÉRCIO LTDA. The registration is held by BRAMSYS INDÚSTRIA E COMÉRCIO LTDA with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.