Pure Global

ERYTHROPOIETIN (EPO) - ANVISA Registration 80102512839

Access comprehensive regulatory information for ERYTHROPOIETIN (EPO) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80102512839 and manufactured by SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS Mร‰DICOS 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 SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED, SIEMENS HEALTHCARE DIAGNOSTICS 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
80102512839
Registration Details
ANVISA Registration Number: 80102512839
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

FAMรLIA MAGLUMI EPO (CLIA)
Risk Class II

Registration Details

80102512839

25351106076202211

04718143000194

Company Information

China
PT: CHINA, REPรšBLICA POPULAR

Dates and Status

Jun 30, 2022

VIGENTE

09/18/2025 19:00:01