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SPINAL FUSION CAGES - ANVISA Registration 80528190039

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 80528190039 and manufactured by NORMMED MED. VE MAK.SAN.TÝC.LTD. ÞTÝ.. The registration is held by NEUROCIÊNCIAS COMÉRCIO E LOCAÇÃO DE PRODUTOS MÉDICOS LTDA with validity until Sep 09, 2029.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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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80528190039
2 Related Devices
Registration Details
ANVISA Registration Number: 80528190039
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Related Devices (2)

Cage Cervical Normmed
Risk Class III

Registration Details

80528190039

25351352469201991

07764288000110

Company Information

Turkey
PT: TURQUIA

Dates and Status

Sep 09, 2019

09/09/2029

09/18/2025 19:00:01

Cage Cervical Normmed
Risk Class III

Registration Details

80528190039

25351352469201991

07764288000110

Dates and Status

Sep 09, 2019

09/09/2029

09/18/2025 19:00:01