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ANVISA registration 80743230124Valid until Aug 17, 2036

Kit de descompressão lombar

ANVISA Registration Number: 80743230124Nexxmed Equipamentos LtdaNexxmed Equipamentos LtdaRisk Class III
Verified
Device names
Technical name
Kit de descompressão lombar
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Commercial name
Kit Cânula Ocidental Endo Plus
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Risk class
Class III
Registration details
Registration Number
80743230124
Process Number
25351100642202604
CNPJ
09135326000109
Company information
Registration Holder
Nexxmed Equipamentos Ltda
Manufacturer
Nexxmed Equipamentos Ltda
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Aug 17, 2026
Validity
17/08/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Kit de descompressão lombar in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80743230124 and manufactured by Nexxmed Equipamentos Ltda. The registration is held by Nexxmed Equipamentos Ltda with validity until Aug 17, 2036.

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.