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SPINAL FUSION CAGES - ANVISA Registration 80102512803

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 80102512803 and manufactured by MEDACTA INTERNATIONAL S.A.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until May 02, 2032.

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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80102512803
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Registration Details
ANVISA Registration Number: 80102512803
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Related Devices (2)

DISPOSITIVO DE FUSÃO TRANSFORAMINAL MECTALIF – TiPEEK
Risk Class III

Registration Details

80102512803

25351716874202166

04718143000194

Company Information

Switzerland
PT: SUÍÇA

Dates and Status

May 02, 2022

02/05/2032

09/18/2025 19:00:01

DISPOSITIVO DE FUSÃO TRANSFORAMINAL MECTALIF – TiPEEK
Risk Class III

Registration Details

80102512803

25351716874202166

04718143000194

Dates and Status

May 02, 2022

02/05/2032

09/18/2025 19:00:01