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ANVISA registration 80722800022Active

CABO/ELETRODO PARA DESFIBRILADOR

ANVISA Registration Number: 80722800022DBI - COMÉRCIO E IMPORTAÇÃO LTDABAISHENG MEDICAL CO LTDRisk Class III
Verified
Device names
Technical name
CABO/ELETRODO PARA DESFIBRILADOR
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Commercial name
Eletrodo para Desfibrilador – marca BluePad
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Risk class
Class III
Registration details
Registration Number
80722800022
Process Number
25351071925202208
CNPJ
07295190000160
Company information
Registration Holder
DBI - COMÉRCIO E IMPORTAÇÃO LTDA
Manufacturer
BAISHENG MEDICAL CO LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Apr 11, 2022
Status
Active
About this record

Access comprehensive regulatory information for CABO/ELETRODO PARA DESFIBRILADOR in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80722800022 and manufactured by BAISHENG MEDICAL CO LTD. The registration is held by DBI - COMÉRCIO E IMPORTAÇÃO LTDA with validity until Apr 11, 2032.

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.