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Trochars - ANVISA Registration 81050760075

Access comprehensive regulatory information for Trochars in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81050760075 and manufactured by TIANXINFU (BEIJING) MEDICAL APPLIANCE 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 AESCULAP AG, KARL STORZ SE & CO. KG, 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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81050760075
Registration Details
ANVISA Registration Number: 81050760075
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Device Details

Dilatador de Tecido Cerebral Descartável Dual Lumen Beijing Medical
Risk Class II

Registration Details

81050760075

25351429609201926

19443457000107

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Aug 19, 2019

VIGENTE

09/18/2025 19:00:01