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Surgical Kit - ANVISA Registration 81000039008

Access comprehensive regulatory information for Surgical Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81000039008 and manufactured by SPINEART SA. The registration is held by Autentica Medical Importação Comercio e Serviços 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 MARDEN MEDICAL LTDA, Humanna Medical Ltda, 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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81000039008
Registration Details
ANVISA Registration Number: 81000039008
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Device Details

Kit Cânulas para Osteoplastia - TEKTONA
Risk Class II

Registration Details

81000039008

25351723589202100

18192496000108

Company Information

SPINEART SA
Switzerland
PT: SUÍÇA

Dates and Status

Nov 18, 2021

VIGENTE

09/18/2025 19:00:01