ANVISA registration 81504799089Valid until Apr 17, 2028PERIPHERAL ANGIOPLASTY BALLOON CATHETER
ANVISA Registration Number: 81504799089PASSROD IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS PARA SAÚDE LTDA - MESHOCKWAVE MEDICAL, INC.Risk Class III
Device names
- Technical name
- PERIPHERAL ANGIOPLASTY BALLOON CATHETER
- Risk class
- Class III
PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Registration details
- Registration Number
- 81504799089
- Process Number
- 25351168379202308
- CNPJ
- 26185222000110
Company information
- Registration Holder
- PASSROD IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS PARA SAÚDE LTDA - ME
- Manufacturer
- SHOCKWAVE MEDICAL, INC.
- Manufacturing Country
- United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
- Publication Date
- Apr 17, 2023
- Validity
- 17/04/2028
- 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 III medical device is registered under ANVISA number 81504799089 and manufactured by SHOCKWAVE MEDICAL, INC.. The registration is held by PASSROD IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS PARA SAÚDE LTDA - ME with validity until Apr 17, 2028.
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