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ANVISA registration 81000030119Valid until Mar 28, 2032

SPINAL FUSION CAGES

ANVISA Registration Number: 81000030119Autentica Medical Importação Comercio e Serviços LTDA-MESPINEARTRisk Class III
Device names
Technical name
SPINAL FUSION CAGES
PT: CAGES PARA FUSÃO DE COLUNA
Commercial name
Família de Cages Lombares Juliet Ti-Life
Risk class
Class III
Registration details
Registration Number
81000030119
Process Number
25351406905202173
CNPJ
18192496000108
Company information
Manufacturer
SPINEART
Manufacturing Country
Switzerland
PT: SUÍÇA
Dates and status
Publication Date
Mar 28, 2022
Validity
28/03/2032
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for SPINAL FUSION CAGES in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81000030119 and manufactured by SPINEART. The registration is held by Autentica Medical Importação Comercio e Serviços LTDA-ME with validity until Mar 28, 2032.

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.