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Orthopedic Insole - ANVISA Registration 10349310036

Access comprehensive regulatory information for Orthopedic Insole in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10349310036 and manufactured by DR. LENOX S.A. The registration is held by VENOSAN BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including ORTHO PAUHER INDUSTRIA COMERCIO E DISTRIBUICOES LTDA, DONGGUAN SUSCONG HEALTHCARE CO.,LTD, 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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10349310036
Registration Details
ANVISA Registration Number: 10349310036
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Device Details

Palmilha de Gel Polรญmero Metatarsal
Risk Class I

Registration Details

10349310036

25351492699202114

02193012000105

Company Information

DR. LENOX S.A
Argentina
PT: ARGENTINA

Dates and Status

May 27, 2021

VIGENTE

09/18/2025 19:00:01