Guide Wire - ANVISA Registration 81231550085

Access comprehensive regulatory information for Guide Wire in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81231550085 and manufactured by manufacturer not specified. The registration is held by Total Life comercio de produtos Medico-Hospitalar LTDA-EPP with validity until Sep 15, 2035.

This page provides complete technical specifications for 2 related devices, 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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81231550085
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Registration Details
ANVISA Registration Number: 81231550085
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Fio guia para Angioplastia
Risk Class IV

Registration Details

81231550085

25351377601202434

21310535000139

Dates and Status

Sep 15, 2025

15/09/2035

09/18/2025 19:00:01

Fio guia para Angioplastia
Risk Class IV

Registration Details

81231550085

25351377601202434

21310535000139

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 15, 2025

15/09/2035

09/18/2025 19:00:01