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ANVISA registration 80416660155Active

CADEIA KAPPA/LAMBDA - RASTREAMENTO, DIAGNÓSTICO OU ESTADIAMENTO DE CÂNCER

ANVISA Registration Number: 80416660155SEBIA IMPORTAÇÕES COMERCIALIZAÇÃO E DISTRIBUIÇÃO DE APARELHOS E REATIVOS PARA DIAGNÓSTICO IN VITRO LTDA.SEBIARisk Class III
Verified
Device names
Technical name
CADEIA KAPPA/LAMBDA - RASTREAMENTO, DIAGNÓSTICO OU ESTADIAMENTO DE CÂNCER
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Commercial name
HYDRAGEL 9 BENCE JONES (SM) MAXI-KIT
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Risk class
Class III
Registration details
Registration Number
80416660155
Process Number
25351154233202539
CNPJ
08576331000186
Company information
Registration Holder
SEBIA IMPORTAÇÕES COMERCIALIZAÇÃO E DISTRIBUIÇÃO DE APARELHOS E REATIVOS PARA DIAGNÓSTICO IN VITRO LTDA.
Manufacturer
SEBIA
Manufacturing Country
France
PT: FRANÇA
Dates and status
Publication Date
Nov 24, 2025
Status
Active
About this record

Access comprehensive regulatory information for CADEIA KAPPA/LAMBDA - RASTREAMENTO, DIAGNÓSTICO OU ESTADIAMENTO DE CÂNCER in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80416660155 and manufactured by SEBIA. The registration is held by SEBIA IMPORTAÇÕES COMERCIALIZAÇÃO E DISTRIBUIÇÃO DE APARELHOS E REATIVOS PARA DIAGNÓSTICO IN VITRO LTDA. with validity until Nov 24, 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.