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Drilling Instrument - ANVISA Registration 81529690001

Access comprehensive regulatory information for Drilling 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 81529690001 and manufactured by EMD ENDOSCOPE DEVICE MANUFACTURING AND SALES LTD. The registration is held by traumaserv - comércio importação e exportação 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 RAZEK EQUIPAMENTOS LTDA, QUADRTECH CORPORATION, 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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81529690001
Registration Details
ANVISA Registration Number: 81529690001
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Device Details

NEUROLINE – PERFURADOR DE CRÂNIO DE USO ÚNICO
Risk Class II

Registration Details

81529690001

25351302679201857

26278328000168

Company Information

Hungary
PT: HUNGRIA

Dates and Status

Jun 25, 2018

VIGENTE

09/18/2025 19:00:01