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Blood Centrifuge - ANVISA Registration 80505289001

Access comprehensive regulatory information for Blood Centrifuge in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80505289001 and manufactured by PROCESS FOR PRF. The registration is held by IMPLANTEC COMÉRCIO E ASSISTÊNCIA TÉCNICA 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 ANDREAS HETTICH GMBH & CO. KG, SHANGHAI LU XIANGYI CENTRIFUGE INSTRUMENT 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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80505289001
Registration Details
ANVISA Registration Number: 80505289001
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Device Details

CENTRÍFUGA PRF
Risk Class II

Registration Details

80505289001

25351803561201841

08510528000112

Company Information

PROCESS FOR PRF
France
PT: FRANÇA

Dates and Status

Apr 29, 2019

VIGENTE

09/18/2025 19:00:01