Probes - ANVISA Registration 81356112329

Access comprehensive regulatory information for Probes in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81356112329 and manufactured by COVIDIEN LLC. The registration is held by CARDINAL HEALTH DO BRASIL 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 WELL LEAD MEDICAL CO, LTD, FRESENIUS KABI AG, 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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81356112329
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Registration Details
ANVISA Registration Number: 81356112329
Janaina dos Santos de Miranda

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Related Devices (2)

PEDI-TUBE SONDA NASOGÁSTRICA PARA ALIMENTACAO ENTERAL ESTERIL KANGAROO
Risk Class II

Registration Details

81356112329

25351552687201842

19585158000107

Company Information

COVIDIEN LLC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Sep 03, 2018

VIGENTE

09/18/2025 19:00:01

PEDI-TUBE SONDA NASOGÁSTRICA PARA ALIMENTACAO ENTERAL ESTERIL KANGAROO
Risk Class II

Registration Details

81356112329

25351552687201842

19585158000107

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Sep 03, 2018

VIGENTE

09/18/2025 19:00:01