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BIOPSY NEEDLE - ANVISA Registration 81504799120

Access comprehensive regulatory information for BIOPSY NEEDLE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81504799120 and manufactured by GUANGZHOU SHENGWEI MEDICAL DEVICES CO., LTD. The registration is held by PASSROD IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS PARA SAÚDE LTDA - ME 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 STERYLAB S.R.L., ZHEJIANG CURAWAY MEDICAL TECHNOLOGY CO., LTD., 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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81504799120
Registration Details
ANVISA Registration Number: 81504799120
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Device Details

Agulha de biópsia Model 112
Risk Class II

Registration Details

81504799120

25351667549202324

26185222000110

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Oct 23, 2023

VIGENTE

09/18/2025 19:00:01