INTRAVASCULAR GUIDE CATHETER - ANVISA Registration 81936210022

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 81936210022 and manufactured by BALT USA LLC. The registration is held by BALT BRASIL PRODUTOS MEDICOS LTDA with validity until Oct 05, 2030.

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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81936210022
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Registration Details
ANVISA Registration Number: 81936210022
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Bainha longa Ballast
Risk Class IV

Registration Details

81936210022

25351040786202181

12236355000244

Company Information

BALT USA LLC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Mar 22, 2021

05/10/2030

09/18/2025 19:00:01

Bainha longa Ballast
Risk Class IV

Registration Details

81936210022

25351040786202181

12236355000244

Company Information

Dates and Status

Mar 22, 2021

05/10/2030

09/18/2025 19:00:01