ANVISA registration 80003920041Active

Blood Centrifuge

Name: Blood Centrifuge — ANVISA registration 80003920041
Creator: DRUCKER DIAGNOSTICS
Keywords: Blood Centrifuge, Centrifuga para Sangue, CENTRÍFUGAS SARSTEDT, 80003920041, Risk Class II, ANVISA registration

ANVISA Registration Number: 80003920041Sarstedt LtdaDRUCKER DIAGNOSTICSRisk Class II

Verified

Device names

Technical name: Blood Centrifuge
Commercial name: CENTRÍFUGAS SARSTEDT
Risk class: Class II

Registration details

Registration Number: 80003920041
Process Number: 25351601118201757
CNPJ: 02661790000181

Company information

Registration Holder: Sarstedt Ltda
Manufacturer: DRUCKER DIAGNOSTICS
Manufacturing Country: United States

Dates and status

Publication Date: Feb 05, 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 80003920041 and manufactured by DRUCKER DIAGNOSTICS. The registration is held by Sarstedt Ltda 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.