ANVISA registration 80689099021ActivePERIPHERAL ANGIOPLASTY BALLOON CATHETER
ANVISA Registration Number: 80689099021BARD BRASIL INDÚSTRIA E COMÉRCIO DE PRODUTOS PARA A SAÚDE LTDA.BARD PERIPHERAL VASCULAR, 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
- 80689099021
- Process Number
- 25351322821202269
- CNPJ
- 10818693000188
Company information
- Registration Holder
- BARD BRASIL INDÚSTRIA E COMÉRCIO DE PRODUTOS PARA A SAÚDE LTDA.
- Manufacturer
- BARD PERIPHERAL VASCULAR, INC.
- Manufacturing Country
- United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
- Publication Date
- Sep 01, 2022
- 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 80689099021 and manufactured by BARD PERIPHERAL VASCULAR, INC.. The registration is held by BARD BRASIL INDÚSTRIA E COMÉRCIO DE PRODUTOS PARA A SAÚDE LTDA. with validity until currently active (VIGENTE).
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