Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

INSTRUMENT FOR ERYTHROCYTE SEDIMENTATION RATE (ESR) - ANVISA Registration 81797610047

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 81797610047 and manufactured by BEIJING SUCCEEDER TECHNOLOGY INC. The registration is held by SALLUS BRASIL PRODUTOS PARA SAUDE IMPORTACAO E EXPORTACAO 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 DIESSE DIAGNÓSTICA SENESE S.P.A, CARETIUM MEDICAL INSTRUMENTS CO.,LIMITED, 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
81797610047
Registration Details
ANVISA Registration Number: 81797610047
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Registration Details

81797610047

25351406584202298

27983599000187

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Oct 27, 2022

VIGENTE

09/18/2025 19:00:01