PERIPHERAL ANGIOPLASTY BALLOON CATHETER
ANVISA Registration Number: 80102519435VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDALEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTDRisk Class II
Device names
- Technical name
- PERIPHERAL ANGIOPLASTY BALLOON CATHETER
- Risk class
- Class II
PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Registration details
- Registration Number
- 80102519435
- Process Number
- 25351124967202674
- CNPJ
- 04718143000194
Company information
- Registration Holder
- VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
- Manufacturer
- LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD
- Manufacturing Country
- China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
- Publication Date
- Aug 03, 2026
- Validity
- VIGENTE
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for PERIPHERAL ANGIOPLASTY BALLOON CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80102519435 and manufactured by LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until currently active (VIGENTE).
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