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Gluteal Prosthesis - ANVISA Registration 80359820006

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 80359820006 and manufactured by SILICONE: INDUSTRIA E COMERCIO DE SILICONE, INSTRUMENTOS E MATERIAIS MEDICOS, CIRURGICOS E HOSPITALARES LTDA. The registration is held by SILICONE: INDUSTRIA E COMERCIO DE SILICONE, INSTRUMENTOS E MATERIAIS MEDICOS, CIRURGICOS E HOSPITALARES LTDA with validity until Aug 15, 2026.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including SILIMED - INDÚSTRIA DE IMPLANTES LTDA, ESTABLISHMENT LABS S.A. (BUILDING B15), 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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80359820006
Registration Details
ANVISA Registration Number: 80359820006
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Device Details

IMPLANTE GLÚTEO DE SILICONE DE SUPERFÍCIE TEXTURIZADA LIFESIL
Risk Class III

Registration Details

80359820006

25351046897201008

07439473000139

Dates and Status

Aug 15, 2011

15/08/2026

09/18/2025 19:00:01