Lumbar decompression kit - ANVISA Registration 81469780063
Access comprehensive regulatory information for Lumbar decompression kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81469780063 and manufactured by SURGITEC COMERCIO E FABRICAÇÃO DE PRODUTOS MEDICOS E HOSPITALARES LTDA - ME. The registration is held by SURGITEC COMERCIO E FABRICAÇÃO DE PRODUTOS MEDICOS E HOSPITALARES LTDA - ME with validity until Feb 14, 2032.
This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including SURGITEC COMERCIO E FABRICAÇÃO DE PRODUTOS MEDICOS E HOSPITALARES LTDA - ME, MARDEN 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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🇧🇷 Brazil Regulatory Expert
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Registration Details
81469780063
25351031074202252
24684423000136
Company Information
Dates and Status
Feb 14, 2022
14/02/2032
09/18/2025 19:00:01
Lumbar decompression kit
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Lumbar decompression kit
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Lumbar decompression kit
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Kit de descompressão lombar
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Kit de descompressão lombar
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Mar 05, 2025