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INFUSION DEVICE - ANVISA Registration 80993370007

Access comprehensive regulatory information for INFUSION DEVICE in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80993370007 and manufactured by LEVENTON S.A.U. The registration is held by UNNO FARMACÊUTICA 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 SMITHS MEDICAL ASD, INC. (MINNEAPOLIS), UNOMEDICAL A/S, 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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80993370007
Registration Details
ANVISA Registration Number: 80993370007
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Device Details

DOSI-FUSER® DOSI-FUSER MULTIFLOW
Risk Class I

Registration Details

80993370007

25351666769202098

08415839000100

Company Information

LEVENTON S.A.U
Spain
PT: ESPANHA

Dates and Status

Jul 30, 2020

VIGENTE

09/18/2025 19:00:01