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Biopsy Device - ANVISA Registration 10349009007

Access comprehensive regulatory information for Biopsy Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10349009007 and manufactured by CARDINAL HEALTH. The registration is held by AUTO SUTURE DO BRASIL 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., Zamar D.O.O., 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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10349009007
Registration Details
ANVISA Registration Number: 10349009007
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Device Details

Sistema de Biópsia por agulha fina SharkCore
Risk Class II

Registration Details

10349009007

25351723341202050

01645409000128

Company Information

CARDINAL HEALTH
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Dec 30, 2020

VIGENTE

09/18/2025 19:00:01