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Disposable Infusion Pump - ANVISA Registration 82777220003

Access comprehensive regulatory information for Disposable Infusion Pump in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 82777220003 and manufactured by ZHEJIANG RUNQIANG MEDICAL INSTRUMENTS CO., LTD. The registration is held by BIOSS PHARMA 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 DAIKEN MEDICAL CO. LTD., ZHEJIANG RUNQIANG MEDICAL INSTRUMENTS 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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82777220003
Registration Details
ANVISA Registration Number: 82777220003
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Device Details

Bomba de Infusão Elastomérica Fluxo Contínuo Bioss
Risk Class I

Registration Details

82777220003

25351378054202412

49551267000166

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Aug 26, 2024

VIGENTE

09/18/2025 19:00:01