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Biopsy Device - ANVISA Registration 80269330003

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 80269330003 and manufactured by Devicor Medical Products de Mexico S de RL de CV. The registration is held by HOSPILINE COMÉRCIO E DISTRIBUIÇÃO DE PRODUTOS MÉDICOS HOSPITALARES LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 related devices, 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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80269330003
2 Related Devices
Registration Details
ANVISA Registration Number: 80269330003
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Related Devices (2)

SONDA MAMMOTOME PARA BIÓPSIA
Risk Class II

Registration Details

80269330003

25351404571201291

07424092000186

Company Information

Dates and Status

Sep 24, 2012

VIGENTE

09/18/2025 19:00:01

SONDA MAMMOTOME PARA BIÓPSIA
Risk Class II

Registration Details

80269330003

25351404571201291

07424092000186

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Sep 24, 2012

VIGENTE

09/18/2025 19:00:01