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INTRAVASCULAR GUIDE CATHETER - ANVISA Registration 80145901967

Access comprehensive regulatory information for INTRAVASCULAR GUIDE CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80145901967 and manufactured by manufacturer not specified. The registration is held by JOHNSON & JOHNSON DO BRASIL INDÚSTRIA E COMÉRCIO DE PRODUTOS PARA SAÚDE LTDA with validity until Nov 04, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including TERUMO CORPORATION, BOSTON SCIENTIFIC CORPORATION - MARLBOROUGH, 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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80145901967
2 Related Devices
Registration Details
ANVISA Registration Number: 80145901967
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Related Devices (2)

GUIDESTAR - Steerable Guiding Sheath
Risk Class IV

Registration Details

80145901967

25351576766202225

54516661000101

Dates and Status

Nov 04, 2024

04/11/2034

09/18/2025 19:00:01

GUIDESTAR - Steerable Guiding Sheath
Risk Class IV

Registration Details

80145901967

25351576766202225

54516661000101

Company Information

OSCOR INC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Nov 04, 2024

04/11/2034

09/18/2025 19:00:01