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Devices - ANVISA Registration 80517530009

Access comprehensive regulatory information for Devices in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80517530009 and manufactured by YONGKANG JINKANG HEALTH EQUIPMENT FACTORY. The registration is held by MASTERMINDS 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 APPLIED MEDICAL TECHNOLOGY, INC, ATOS MEDICAL AB, 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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80517530009
Registration Details
ANVISA Registration Number: 80517530009
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Device Details

kit ventosa dux
Risk Class I

Registration Details

80517530009

25351126945202053

05381531000195

Company Information

China
PT: CHINA, REPรšBLICA POPULAR

Dates and Status

May 14, 2020

VIGENTE

09/18/2025 19:00:01