Pure Global AI
ANVISA registration 80517530009Active

Devices

ANVISA Registration Number: 80517530009MASTERMINDS LTDAYONGKANG JINKANG HEALTH EQUIPMENT FACTORYRisk Class I
Verified
Device names
Technical name
Devices
View exact technical-name matches →
PT: Dispositivos
Commercial name
kit ventosa dux
View exact commercial-name matches →
Risk class
Class I
Registration details
Registration Number
80517530009
Process Number
25351126945202053
CNPJ
05381531000195
Company information
Registration Holder
MASTERMINDS LTDA
Manufacturer
YONGKANG JINKANG HEALTH EQUIPMENT FACTORY
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
May 14, 2020
Status
Active
Official value: VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

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 shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.