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Injectable PEEK - ANVISA Registration 80383789004

Access comprehensive regulatory information for Injectable PEEK in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80383789004 and manufactured by NUXEN SRL. The registration is held by TALDEN IMPORTAÇÃO E COMÉRCIO DE EQUIPAMENTOS PARA A SAÚDE LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 1 companies making the same product including CELMAT INDUSTRIA DE MATERIAIS E ARTEFATOS CERAMICOS PARA USO ODONTOLOGICO E INDUSTRIAL LTDA-EPP, and 1 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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80383789004
Registration Details
ANVISA Registration Number: 80383789004
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Device Details

DEFLEX PEEK
Risk Class II

Registration Details

80383789004

25351040010202081

07897781000108

Company Information

NUXEN SRL
Argentina
PT: ARGENTINA

Dates and Status

Mar 16, 2020

VIGENTE

09/18/2025 19:00:01

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