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SPACER - ANVISA Registration 10387179005

Access comprehensive regulatory information for SPACER in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10387179005 and manufactured by PLASTIC WAY PRODUTOS PARA A SAÚDE LTDA. The registration is held by PLASTIC WAY PRODUTOS PARA A SAÚDE 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 PLASTIC WAY PRODUTOS PARA A SAÚDE LTDA, HUIZHOU KAIYI TECHNOLOGY 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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10387179005
Registration Details
ANVISA Registration Number: 10387179005
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Device Details

CÂMARA RETRÁTIL
Risk Class II

Registration Details

10387179005

25351290534202100

01202521000194

Company Information

Brazil
PT: BRASIL

Dates and Status

Apr 15, 2021

VIGENTE

09/18/2025 19:00:01