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Surgical Equipment for Discectomy - ANVISA Registration 81050769011

Access comprehensive regulatory information for Surgical Equipment for Discectomy in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81050769011 and manufactured by BIOPSYBELL S.R.L.. The registration is held by GUSMED DO BRASIL COMERCIO E LOCAÇÃO DE PRODUTOS MEDICOS LTDA - EPP 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 MARDEN MEDICAL LTDA, SEAWON MEDITECH 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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81050769011
Registration Details
ANVISA Registration Number: 81050769011
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Device Details

DISPOSITIVO PERCUTÂNEO DE REMOÇÃO DE NÚCLEO PULPOSO DISKOM
Risk Class II

Registration Details

81050769011

25351821648202104

19443457000107

Company Information

BIOPSYBELL S.R.L.
Italy
PT: ITÁLIA

Dates and Status

Jan 14, 2021

VIGENTE

09/18/2025 19:00:01