ANVISA registration 10256400075Valid until Dec 28, 2035Beam guide catheter for peripheral atherectomy laser system
ANVISA Registration Number: 10256400075BIOMEDICAL PRODUTOS CIENTIFICOS MEDICOS E HOSPITALARES S ASPECTRANETICS CORPORATIONRisk Class III
Device names
- Technical name
- Beam guide catheter for peripheral atherectomy laser system
- Risk class
- Class III
PT: Cateter-guia de feixe para sistema de laser de aterectomia, periférico
Registration details
- Registration Number
- 10256400075
- Process Number
- 25351644440202076
- 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
- Jul 20, 2020
- Validity
- 28/12/2035
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for Beam guide catheter for peripheral atherectomy laser system in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10256400075 and manufactured by SPECTRANETICS CORPORATION. The registration is held by BIOMEDICAL PRODUTOS CIENTIFICOS MEDICOS E HOSPITALARES S A with validity until Dec 28, 2035.
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