ANVISA registration 10256400043ActivePERIPHERAL ANGIOPLASTY BALLOON CATHETER
ANVISA Registration Number: 10256400043BIOMEDICAL PRODUTOS CIENTIFICOS MEDICOS E HOSPITALARES S ASPECTRANETICS CORPORATIONRisk Class II
Device names
- Technical name
- PERIPHERAL ANGIOPLASTY BALLOON CATHETER
- Risk class
- Class II
PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Registration details
- Registration Number
- 10256400043
- Process Number
- 25351653930201768
- CNPJ
- 19848316000166
Company information
- Registration Holder
- BIOMEDICAL PRODUTOS CIENTIFICOS MEDICOS E HOSPITALARES S A
- Manufacturer
- SPECTRANETICS CORPORATION
- Manufacturing Country
- United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
- Publication Date
- Feb 19, 2018
- 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 10256400043 and manufactured by SPECTRANETICS CORPORATION. The registration is held by BIOMEDICAL PRODUTOS CIENTIFICOS MEDICOS E HOSPITALARES S A with validity until currently active (VIGENTE).
This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.