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Kit for Infusion Pump - ANVISA Registration 80384380056

Access comprehensive regulatory information for Kit for Infusion Pump in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80384380056 and manufactured by BAYER MEDICAL CARE INC.. The registration is held by BAYER S.A. 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 SHANDONG ANDE HEALTHCARE APPARATUS CO., LTD., SHENZHEN MAIWEI BIOTECH 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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80384380056
Registration Details
ANVISA Registration Number: 80384380056
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Device Details

SDS MP1 - Kit Multi-Paciente
Risk Class II

Registration Details

80384380056

25351057479201701

18459628000115

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

May 17, 2017

VIGENTE

09/18/2025 19:00:01