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ANVISA registration 80356130216Valid until Oct 06, 2035

Lumbar decompression kit

ANVISA Registration Number: 80356130216RAZEK EQUIPAMENTOS LTDARAZEK EQUIPAMENTOS LTDARisk Class III
Verified
Device names
Technical name
Lumbar decompression kit
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PT: Kit de descompressão lombar
Commercial name
EndoSpine Dual
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Risk class
Class III
Registration details
Registration Number
80356130216
Process Number
25351121371202531
CNPJ
07489080000130
Company information
Registration Holder
RAZEK EQUIPAMENTOS LTDA
Manufacturer
RAZEK EQUIPAMENTOS LTDA
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Oct 06, 2025
Validity
06/10/2035
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 III medical device is registered under ANVISA number 80356130216 and manufactured by RAZEK EQUIPAMENTOS LTDA. The registration is held by RAZEK EQUIPAMENTOS LTDA with validity until Oct 06, 2035.

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.