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BIOPSY NEEDLE - ANVISA Registration 80485600001

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 80485600001 and manufactured by STERYLAB S.R.L.. The registration is held by INTERSUPPLY COMÉRCIO IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS PARA A SAÚDE LTDA 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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80485600001
Registration Details
ANVISA Registration Number: 80485600001
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Device Details

AGULHAS PARA BIÓPSIAS HEMATOLÓGICAS DE MEDULA ÓSSEA
Risk Class II

Registration Details

80485600001

25351062227201009

07410967000190

Company Information

STERYLAB S.R.L.
Italy
PT: ITÁLIA

Dates and Status

Mar 28, 2011

VIGENTE

09/18/2025 19:00:01