Pure Global AI
ANVISA registration 80188200002Active

Guide Wire

ANVISA Registration Number: 80188200002IMPORMEDICA IMPORTACAO, EXPORTACAO, SERVICOS DE MANUTENCAO DE EQUIPAMENTOS LTDA - EPPSHAILI ENDOSCOPYRisk Class II
Verified
Device names
Technical name
Guide Wire
View exact technical-name matches →
PT: Fio Guia
Commercial name
NEG GUIDE WIRE
View exact commercial-name matches →
Risk class
Class II
Registration details
Registration Number
80188200002
Process Number
25351321067201031
CNPJ
00566693000184
Company information
Registration Holder
IMPORMEDICA IMPORTACAO, EXPORTACAO, SERVICOS DE MANUTENCAO DE EQUIPAMENTOS LTDA - EPP
Manufacturer
SHAILI ENDOSCOPY
Manufacturing Country
India
PT: ÍNDIA
Dates and status
Publication Date
Mar 26, 2012
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Guide Wire in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80188200002 and manufactured by SHAILI ENDOSCOPY. The registration is held by IMPORMEDICA IMPORTACAO, EXPORTACAO, SERVICOS DE MANUTENCAO DE EQUIPAMENTOS LTDA - EPP 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.