SPINAL FUSION CAGES - ANVISA Registration 80444810013

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 80444810013 and manufactured by manufacturer not specified. The registration is held by HIGHRIDGE MEDICAL BRASIL LTDA with validity until May 27, 2028.

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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80444810013
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Registration Details
ANVISA Registration Number: 80444810013
Janaina dos Santos de Miranda

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Related Devices (2)

GAIOLA LOMBAR ROI-A
Risk Class III

Registration Details

80444810013

25351334411201014

08954683000128

Company Information

Dates and Status

May 27, 2013

27/05/2028

09/18/2025 19:00:01

GAIOLA LOMBAR ROI-A
Risk Class III

Registration Details

80444810013

25351334411201014

08954683000128

Company Information

LDR MEDICAL
France
PT: FRANÇA

Dates and Status

May 27, 2013

27/05/2028

09/18/2025 19:00:01