ANVISA registration 82392089013ActivePERIPHERAL ANGIOPLASTY BALLOON CATHETER
ANVISA Registration Number: 82392089013EUROGREEN DISTRIBUIDORA DE PRODUTOS HOSPITALARES LTDAREFLOW MEDICAL, INC.Risk Class II
Device names
- Technical name
- PERIPHERAL ANGIOPLASTY BALLOON CATHETER
- Risk class
- Class II
PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Registration details
- Registration Number
- 82392089013
- Process Number
- 25351235614202518
- CNPJ
- 41194659000103
Company information
- Registration Holder
- EUROGREEN DISTRIBUIDORA DE PRODUTOS HOSPITALARES LTDA
- Manufacturer
- REFLOW MEDICAL, INC.
- Manufacturing Country
- United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
- Publication Date
- Dec 29, 2025
- Status
- Active
Official value: VIGENTE
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 82392089013 and manufactured by REFLOW MEDICAL, INC.. The registration is held by EUROGREEN DISTRIBUIDORA DE PRODUTOS HOSPITALARES LTDA with validity until currently active (VIGENTE).
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