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ANVISA registration 80380269002Active

Blood Centrifuge

ANVISA Registration Number: 80380269002MEDSYSTEMS COMERCIO, IMPORTACAO E EXPORTACAO LTDA - EPPREGEN LAB SARisk Class II
Verified
Device names
Technical name
Blood Centrifuge
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PT: Centrifuga para Sangue
Commercial name
RegenCentri
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Risk class
Class II
Registration details
Registration Number
80380269002
Process Number
25351303269201823
CNPJ
05273422000154
Company information
Registration Holder
MEDSYSTEMS COMERCIO, IMPORTACAO E EXPORTACAO LTDA - EPP
Manufacturer
REGEN LAB SA
Manufacturing Country
Switzerland
PT: SUÍÇA
Dates and status
Publication Date
Sep 03, 2018
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

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 80380269002 and manufactured by REGEN LAB SA. The registration is held by MEDSYSTEMS COMERCIO, IMPORTACAO E EXPORTACAO LTDA - EPP with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.