Pure Global AI
ANVISA registration 81251089026Active

FIO GUIA DE USO GERAL, NÃO VASCULAR

ANVISA Registration Number: 81251089026ENDOSURG INDUSTRIA, COMERCIO, IMPORTACAO DISTRIBUICAO E LOCACAO DE MATERIAIS MEDICOS LTDAMEDITECH DEVICES PVT LTDRisk Class II
Verified
Device names
Technical name
FIO GUIA DE USO GERAL, NÃO VASCULAR
View exact technical-name matches →
Commercial name
Fio Guia PTFE Endosurg
View exact commercial-name matches →
Risk class
Class II
Registration details
Registration Number
81251089026
Process Number
25351084168202658
CNPJ
21368015000187
Company information
Registration Holder
ENDOSURG INDUSTRIA, COMERCIO, IMPORTACAO DISTRIBUICAO E LOCACAO DE MATERIAIS MEDICOS LTDA
Manufacturer
MEDITECH DEVICES PVT LTD
Manufacturing Country
India
PT: ÍNDIA
Dates and status
Publication Date
Jun 01, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for FIO GUIA DE USO GERAL, NÃO VASCULAR in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81251089026 and manufactured by MEDITECH DEVICES PVT LTD. The registration is held by ENDOSURG INDUSTRIA, COMERCIO, IMPORTACAO DISTRIBUICAO E LOCACAO DE MATERIAIS MEDICOS LTDA 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.