Guide Wire - ANVISA Registration 81231550017

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 81231550017 and manufactured by SP MEDICAL A/S. The registration is held by Total Life comercio de produtos Medico-Hospitalar LTDA-EPP 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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81231550017
Registration Details
ANVISA Registration Number: 81231550017
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Fio Guia Teflonado Accoat
Risk Class II

Registration Details

81231550017

25351125771201706

21310535000139

Company Information

SP MEDICAL A/S
Denmark
PT: DINAMARCA

Dates and Status

May 22, 2017

VIGENTE

09/18/2025 19:00:01