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SPACER - ANVISA Registration 10343200032

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 10343200032 and manufactured by Taian Dalu Medical Instrument Co., Ltd.. The registration is held by INCOTERM SOLUÇÕES EM MEDIÇÃO 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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10343200032
Registration Details
ANVISA Registration Number: 10343200032
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Device Details

ESPAÇADOR E100
Risk Class I

Registration Details

10343200032

25351042774201701

87156352000119

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

May 22, 2017

VIGENTE

09/18/2025 19:00:01