Cannulas - ANVISA Registration 10320090022

Access comprehensive regulatory information for Cannulas in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10320090022 and manufactured by SALTER LABS DE MEXICO S.A. DE C.V.. The registration is held by HOMED EQUIPAMENTOS MEDICO HOSPITALAR LTDA - EPP with validity until currently active (VIGENTE).

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 TRACOE MEDICAL GMBH, MARDEN MEDICAL LTDA, 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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10320090022
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Registration Details
ANVISA Registration Number: 10320090022
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

CÂNULA PARA DIAGNÓSTICO DE APNEIA SALTER LABS
Risk Class I

Registration Details

10320090022

25351206290201341

64835721000102

Company Information

Mexico
PT: MÉXICO

Dates and Status

Aug 19, 2013

VIGENTE

09/18/2025 19:00:01

CÂNULA PARA DIAGNÓSTICO DE APNEIA SALTER LABS
Risk Class I

Registration Details

10320090022

25351206290201341

64835721000102

Company Information

SALTER LABS
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 19, 2013

VIGENTE

09/18/2025 19:00:01