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Gluteal Prosthesis - ANVISA Registration 80588390012

Access comprehensive regulatory information for Gluteal Prosthesis in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80588390012 and manufactured by manufacturer not specified. The registration is held by ESTABLISHMENT LABS BRASIL PRODUTOS PARA SAUDE LTDA with validity until Nov 16, 2032.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including SILICONE: INDUSTRIA E COMERCIO DE SILICONE, INSTRUMENTOS E MATERIAIS MEDICOS, CIRURGICOS E HOSPITALARES LTDA, SILIMED - INDÚSTRIA DE IMPLANTES LTDA, 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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80588390012
2 Related Devices
Registration Details
ANVISA Registration Number: 80588390012
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Related Devices (2)

GLUTEALARMONIC™ SILKSURFACE™ MOTIVA IMPLANTS MATRIX™ WITH ZEN - IMPLANTES ESTEREIS DE SILICONE PARA GLÚTEOS
Risk Class III

Registration Details

80588390012

25351018612202132

08290164000102

Company Information

Dates and Status

Nov 16, 2022

16/11/2032

09/18/2025 19:00:01

GLUTEALARMONIC™ SILKSURFACE™ MOTIVA IMPLANTS MATRIX™ WITH ZEN - IMPLANTES ESTEREIS DE SILICONE PARA GLÚTEOS
Risk Class III

Registration Details

80588390012

25351018612202132

08290164000102

Company Information

Costa Rica
PT: COSTA RICA

Dates and Status

Nov 16, 2022

16/11/2032

09/18/2025 19:00:01