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INSTRUMENT FOR ERYTHROCYTE SEDIMENTATION RATE (ESR) - ANVISA Registration 80785070271

Access comprehensive regulatory information for INSTRUMENT FOR ERYTHROCYTE SEDIMENTATION RATE (ESR) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80785070271 and manufactured by CARETIUM MEDICAL INSTRUMENTS CO.,LIMITED. The registration is held by Vida Biotecnologia Ltda - ME 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 DIESSE DIAGNÓSTICA SENESE S.P.A, BEIJING SUCCEEDER TECHNOLOGY INC, 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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80785070271
Registration Details
ANVISA Registration Number: 80785070271
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Device Details

FAMÍLIA DE ANALISADORES DE VELOCIDADE DE HEMOSEDIMENTAÇÃO (CARETIUM)
Risk Class II

Registration Details

80785070271

25351083475202531

11308834000185

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jul 07, 2025

VIGENTE

09/18/2025 19:00:01