ULTRASENSITIVE C-REACTIVE PROTEIN - ANVISA Registration 81325990355

Access comprehensive regulatory information for ULTRASENSITIVE C-REACTIVE PROTEIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81325990355 and manufactured by HANGZHOU ALLTEST BIOTECH CO. LTD. The registration is held by QR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including LABTEST DIAGNOSTICA S/A, BIOSYSTEMS S.A., 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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81325990355
Registration Details
ANVISA Registration Number: 81325990355
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

CRP FIA (Sangue Total/Soro/Plasma)
Risk Class II

Registration Details

81325990355

25351134793202496

19933144000129

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Aug 05, 2024

VIGENTE

09/18/2025 19:00:01