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ANVISA registration 80740950181Valid until Mar 23, 2036

Catheters

ANVISA Registration Number: 80740950181MERIT MEDICAL COMERCIALIZAÇÃO, DISTRIBUIÇÃO, IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS HOSPITALARES LTDAMERIT MEDICAL SYSTEMS, INC.Risk Class IV
Verified
Device names
Technical name
Catheters
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PT: Cateteres
Commercial name
Cateter para hemodiálise BioFlo DuraMax®
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Risk class
Class IV
Registration details
Registration Number
80740950181
Process Number
25351437014202410
CNPJ
13200579000188
Company information
Registration Holder
MERIT MEDICAL COMERCIALIZAÇÃO, DISTRIBUIÇÃO, IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS HOSPITALARES LTDA
Manufacturer
MERIT MEDICAL SYSTEMS, INC.
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Mar 23, 2026
Validity
23/03/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Catheters in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80740950181 and manufactured by MERIT MEDICAL SYSTEMS, INC.. The registration is held by MERIT MEDICAL COMERCIALIZAÇÃO, DISTRIBUIÇÃO, IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS HOSPITALARES LTDA with validity until Mar 23, 2036.

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.