SPINAL FUSION CAGES - ANVISA Registration 80384860011

Access comprehensive regulatory information for SPINAL FUSION CAGES in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80384860011 and manufactured by CENTINEL SPINE, INC.. The registration is held by CROMO LIFE DISTRIBUIDORA DE MATERIAIS HOSPITALARES LTDA - ME with validity until Nov 27, 2033.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including AESCULAP AG, OSTEOMED S.A, 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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80384860011
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Registration Details
ANVISA Registration Number: 80384860011
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Prodisc C VIVO – Prótese de disco cervical
Risk Class IV

Registration Details

80384860011

25351473957202236

08299064000147

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Nov 27, 2023

27/11/2033

09/18/2025 19:00:01

Prodisc C VIVO – Prótese de disco cervical
Risk Class IV

Registration Details

80384860011

25351473957202236

08299064000147

Dates and Status

Nov 27, 2023

27/11/2033

09/18/2025 19:00:01