SPACER - ANVISA Registration 10387170052

Access comprehensive regulatory information for SPACER in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10387170052 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 similar products found using AI-powered semantic search, 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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10387170052
Registration Details
ANVISA Registration Number: 10387170052
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

ESPAÇADOR PARA AEROSSOL PLASTIC WAY
Risk Class I

Registration Details

10387170052

25351658670202284

01202521000194

Company Information

Brazil
PT: BRASIL

Dates and Status

Jan 02, 2023

VIGENTE

09/18/2025 19:00:01