CARDIOVASCULAR GUIDE WIRE - ANVISA Registration 80146501715

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 80146501715 and manufactured by ABBOTT MEDICAL. The registration is held by ABBOTT LABORATORIOS DO BRASIL LTDA with validity until Oct 18, 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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80146501715
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Registration Details
ANVISA Registration Number: 80146501715
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

HI-TORQUE PROGRESS GUIDE WIRE
Risk Class IV

Registration Details

80146501715

25351047813201048

56998701000116

Company Information

ABBOTT MEDICAL
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Oct 18, 2010

18/10/2035

09/18/2025 19:00:01

HI-TORQUE PROGRESS GUIDE WIRE
Risk Class IV

Registration Details

80146501715

25351047813201048

56998701000116

Company Information

Dates and Status

Oct 18, 2010

18/10/2035

09/18/2025 19:00:01