SPINAL FUSION CAGES - ANVISA Registration 80003890120

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 80003890120 and manufactured by manufacturer not specified. The registration is held by CANADA CENTRAL DE NEGOCIOS DO BRASIL LTDA with validity until Apr 15, 2029.

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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80003890120
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Registration Details
ANVISA Registration Number: 80003890120
Janaina dos Santos de Miranda

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Related Devices (2)

CAGE INTERSOMÁTICO PARA COLUNA VERTEBRAL EM PEEK MAHE
Risk Class III

Registration Details

80003890120

25351604535201808

01911022000176

Company Information

Dates and Status

Apr 15, 2019

15/04/2029

09/18/2025 19:00:01

CAGE INTERSOMÁTICO PARA COLUNA VERTEBRAL EM PEEK MAHE
Risk Class III

Registration Details

80003890120

25351604535201808

01911022000176

Company Information

MAHE MEDICAL GMBH
Germany
PT: ALEMANHA

Dates and Status

Apr 15, 2019

15/04/2029

09/18/2025 19:00:01