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Bone Drilling Burs - ANVISA Registration 81704419002

Access comprehensive regulatory information for Bone Drilling Burs in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81704419002 and manufactured by TIANJIN KANGER MEDICAL TREATMENT APPARATUS CO., LTD. The registration is held by MEDSITE EQUIPAMENTOS E PRODUTOS PARA SAÚDE LTDA - ME 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 MEDTRONIC XOMED INC, MEDTRONIC, INC., 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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81704419002
Registration Details
ANVISA Registration Number: 81704419002
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Device Details

Perfurador Craniano Descartável
Risk Class II

Registration Details

81704419002

25351039931202513

29136675000144

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Mar 31, 2025

VIGENTE

09/18/2025 19:00:01