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SPACER - ANVISA Registration 80275310056

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 80275310056 and manufactured by TAIAN DALU MEDICAL INSTRUMENT CO., LTD.. The registration is held by ACCUMED PRODUTOS MÉDICO HOSPITALARES 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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80275310056
Registration Details
ANVISA Registration Number: 80275310056
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Device Details

Espaçador G-Tech
Risk Class I

Registration Details

80275310056

25351513755201456

06105362000123

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Dec 15, 2014

VIGENTE

09/18/2025 19:00:01