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Biopsy Instrument - ANVISA Registration 10216719021

Access comprehensive regulatory information for Biopsy Instrument in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10216719021 and manufactured by INVIVO CORPORATION. The registration is held by PHILIPS MEDICAL SYSTEMS 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., CHAMFOND BIOTECH 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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10216719021
Registration Details
ANVISA Registration Number: 10216719021
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Device Details

Kit de bióPsia para mama \ NMRF 358 \ dS Breast Adapt 16ch Intrv Kit
Risk Class II

Registration Details

10216719021

25351894398202032

58295213000178

Company Information

INVIVO CORPORATION
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Oct 01, 2020

VIGENTE

09/18/2025 19:00:01