Pure Global AI
ANVISA registration 80984199007Active

Guide Wire

ANVISA Registration Number: 80984199007GADALI MEDICAL COMÉRCIO DE PRODUTOS MÉDICO-HOSPITALAR LTDA. MESHUNMEI MEDICAL Co., LtdRisk Class II
Verified
Device names
Technical name
Guide Wire
View exact technical-name matches →
PT: Fio Guia
Commercial name
Fio Guia Hidrofílico Periférico
View exact commercial-name matches →
Risk class
Class II
Registration details
Registration Number
80984199007
Process Number
25351415833202074
CNPJ
06143957000173
Company information
Registration Holder
GADALI MEDICAL COMÉRCIO DE PRODUTOS MÉDICO-HOSPITALAR LTDA. ME
Manufacturer
SHUNMEI MEDICAL Co., Ltd
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Nov 12, 2020
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 80984199007 and manufactured by SHUNMEI MEDICAL Co., Ltd. The registration is held by GADALI MEDICAL COMÉRCIO DE PRODUTOS MÉDICO-HOSPITALAR LTDA. ME 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.