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Cough stimulation system - ANVISA Registration 81187719001

Access comprehensive regulatory information for Cough stimulation system in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81187719001 and manufactured by MEDICAL PRODUCTS RESEARCH S.R.L.. The registration is held by VIVISOL BRASIL EQUIPAMENTOS MÉDICOS HOSPITALARES LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 1 companies making the same product including SEOIL PACIFIC CORP., and 1 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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81187719001
Registration Details
ANVISA Registration Number: 81187719001
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Device Details

Dispositivo para eliminação de secreções das vias aéreas e assistente de tosse KINEX
Risk Class II

Registration Details

81187719001

25351459008202413

20513627000153

Company Information

Italy
PT: ITÁLIA

Dates and Status

Feb 17, 2025

VIGENTE

09/18/2025 19:00:01

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