Tracheostomy Kit - ANVISA Registration 80228990179

Access comprehensive regulatory information for Tracheostomy Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80228990179 and manufactured by SMITHS MEDICAL ASD, INC. (MINNEAPOLIS). The registration is held by ICU MEDICAL DO BRASIL PRODUTOS HOSPITALARES LTDA 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 SMITHS MEDICAL ASD, INC. (MINNEAPOLIS), ICU MEDICAL, INC., 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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80228990179
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Registration Details
ANVISA Registration Number: 80228990179
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Tubos de traqueostomia com cânula interna lisa e Cuff Soft Seal®
Risk Class II

Registration Details

80228990179

25351148300202071

06019570000100

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jul 13, 2020

VIGENTE

09/18/2025 19:00:01

Tubos de traqueostomia com cânula interna lisa e Cuff Soft Seal®
Risk Class II

Registration Details

80228990179

25351148300202071

06019570000100

Company Information

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

Dates and Status

Jul 13, 2020

VIGENTE

09/18/2025 19:00:01