INTRAVASCULAR GUIDE CATHETER - ANVISA Registration 81248520015

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 81248520015 and manufactured by manufacturer not specified. The registration is held by Penumbra Latin America Distribuidora de Equipamentos e Produtos Médicos Ltda with validity until Jul 29, 2029.

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 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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81248520015
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Registration Details
ANVISA Registration Number: 81248520015
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

CATETER DE ACESSO INTRACRANIANO NEURON MAX - PONTA ANGULADA
Risk Class IV

Registration Details

81248520015

25351279658201910

21873761000128

Dates and Status

Jul 29, 2019

29/07/2029

09/18/2025 19:00:01

CATETER DE ACESSO INTRACRANIANO NEURON MAX - PONTA ANGULADA
Risk Class IV

Registration Details

81248520015

25351279658201910

21873761000128

Company Information

PENUMBRA, INC.
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jul 29, 2019

29/07/2029

09/18/2025 19:00:01