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Instrument Kit - ANVISA Registration 81050760067

Access comprehensive regulatory information for Instrument Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81050760067 and manufactured by ZHEJIANG TIANSONG MEDICAL INSTRUMENT Co., Ltd. The registration is held by GUSMED DO BRASIL COMERCIO E LOCAÇÃO DE PRODUTOS MEDICOS LTDA - EPP with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including MARDEN MEDICAL LTDA, LIMA CORPORATE S.P.A, 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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81050760067
Registration Details
ANVISA Registration Number: 81050760067
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Device Details

Kit Instrumental para Ventriculoscopia Tiansong
Risk Class I

Registration Details

81050760067

25351399524201914

19443457000107

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jul 18, 2019

VIGENTE

09/18/2025 19:00:01