ANVISA registration 80102513220Valid until Apr 01, 2034ENDOPROSTHESIS (VASCULAR)
ANVISA Registration Number: 80102513220VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDALIFETECH SCIENTIFIC (SHENZHEN) CO., LTD.Risk Class IV
Device names
- Technical name
- ENDOPROSTHESIS (VASCULAR)
- Commercial name
- Sistema de Endoprótese de Bifurcação Ilíaca G-iliac
- Risk class
- Class IV
PT: ENDOPRÓTESE (VASCULAR)
Registration details
- Registration Number
- 80102513220
- Process Number
- 25351288101202348
- CNPJ
- 04718143000194
Company information
- Registration Holder
- VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
- Manufacturer
- LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD.
- Manufacturing Country
- China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
- Publication Date
- Apr 01, 2024
- Validity
- 01/04/2034
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for ENDOPROSTHESIS (VASCULAR) in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80102513220 and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Apr 01, 2034.
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