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ANVISA registration 10256400044Active

Guide Wire

ANVISA Registration Number: 10256400044BIOMEDICAL PRODUTOS CIENTIFICOS MEDICOS E HOSPITALARES S ASP MEDICAL A/SRisk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Fio Guia Hidrofílico
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Risk class
Class II
Registration details
Registration Number
10256400044
Process Number
25351292749201851
CNPJ
19848316000166
Company information
Registration Holder
BIOMEDICAL PRODUTOS CIENTIFICOS MEDICOS E HOSPITALARES S A
Manufacturer
SP MEDICAL A/S
Manufacturing Country
Denmark
PT: DINAMARCA
Dates and status
Publication Date
May 27, 2019
Status
Active
Official value: VIGENTE
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 10256400044 and manufactured by SP MEDICAL A/S. The registration is held by BIOMEDICAL PRODUTOS CIENTIFICOS MEDICOS E HOSPITALARES S A 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.