ANVISA registration 82016170006ActiveCOMBINED PARAMETERS IN THE SAME PRODUCT - CLASS II
ANVISA Registration Number: 82016170006EXTRA MEDICAL DIAGNOSTICOS LTDAJIANGSU KONSUNG BIO MEDICAL SCIENCE AND TECHNOLOGY CO., LTDRisk Class II
Device names
- Technical name
- COMBINED PARAMETERS IN THE SAME PRODUCT - CLASS II
- Commercial name
- Cartão de Teste Ureia, Creatinina e Ácido Úrico - Analisador Bioquímico Seco
- Risk class
- Class II
PT: PARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE II
Registration details
- Registration Number
- 82016170006
- Process Number
- 25351867164202101
- CNPJ
- 34011468000101
Company information
- Registration Holder
- EXTRA MEDICAL DIAGNOSTICOS LTDA
- Manufacturing Country
- China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
- Publication Date
- Aug 19, 2021
- Validity
- VIGENTE
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for COMBINED PARAMETERS IN THE SAME PRODUCT - CLASS II in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82016170006 and manufactured by JIANGSU KONSUNG BIO MEDICAL SCIENCE AND TECHNOLOGY CO., LTD. The registration is held by EXTRA MEDICAL DIAGNOSTICOS LTDA with validity until currently active (VIGENTE).
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