CARDIOVASCULAR GUIDE WIRE - ANVISA Registration 80012280073

Access comprehensive regulatory information for CARDIOVASCULAR 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 80012280073 and manufactured by TERUMO CORPORATION. The registration is held by TERUMO MEDICAL DO BRASIL LTDA. with validity until Sep 26, 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 ABBOTT MEDICAL, COOK INCORPORATED, 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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80012280073
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Registration Details
ANVISA Registration Number: 80012280073
Janaina dos Santos de Miranda

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Related Devices (2)

FIO GUIA RADIOFOCUS GLIDEWIRE TERUMO
Risk Class IV

Registration Details

80012280073

25351176974200527

03129105000133

Company Information

TERUMO CORPORATION
Japan
PT: JAPÃO

Dates and Status

Sep 26, 2005

26/09/2035

09/18/2025 19:00:01

FIO GUIA RADIOFOCUS GLIDEWIRE TERUMO
Risk Class IV

Registration Details

80012280073

25351176974200527

03129105000133

Company Information

Dates and Status

Sep 26, 2005

26/09/2035

09/18/2025 19:00:01