Guide Wire - ANVISA Registration 10256400055

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 10256400055 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 provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, SP MEDICAL A/S, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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10256400055
Registration Details
ANVISA Registration Number: 10256400055
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Fio Guia revestido de PTFE
Risk Class II

Registration Details

10256400055

25351389055201836

19848316000166

Company Information

SP MEDICAL A/S
Denmark
PT: DINAMARCA

Dates and Status

Nov 12, 2018

VIGENTE

09/18/2025 19:00:01