ANVISA registration 80102512237Valid until Jun 24, 2029Self-test instrument for glucose
ANVISA Registration Number: 80102512237VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDATIANJIN EMPECS MEDICAL DEVICE CO., LTD.Risk Class III
Device names
- Technical name
- Self-test instrument for glucose
- Commercial name
- Família de Monitores de Glicose Sanguínea Empecs Série MM
- Risk class
- Class III
PT: Instrumento autoteste para glicose
Registration details
- Registration Number
- 80102512237
- Process Number
- 25351076288201909
- CNPJ
- 04718143000194
Company information
- Registration Holder
- VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
- Manufacturer
- TIANJIN EMPECS MEDICAL DEVICE CO., LTD.
- Manufacturing Country
- China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
- Publication Date
- Jun 24, 2019
- Validity
- 24/06/2029
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for Self-test instrument for glucose in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80102512237 and manufactured by TIANJIN EMPECS MEDICAL DEVICE CO., LTD.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Jun 24, 2029.
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