PERIPHERAL ANGIOPLASTY BALLOON CATHETER
ANVISA Registration Number: 80202919025TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDANEXSTEP MEDICALRisk Class II
Device names
- Technical name
- PERIPHERAL ANGIOPLASTY BALLOON CATHETER
- Commercial name
- Cateter Balão de Dilatação para PTA AllInCath 035M
- Risk class
- Class II
PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Registration details
- Registration Number
- 80202919025
- Process Number
- 25351210292202502
- CNPJ
- 05638301000169
Company information
- Registration Holder
- TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDA
- Manufacturer
- NEXSTEP MEDICAL
- Manufacturing Country
- France
PT: FRANÇA
Dates and status
- Publication Date
- Nov 24, 2025
- 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 80202919025 and manufactured by NEXSTEP MEDICAL. The registration is held by TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDA with validity until currently active (VIGENTE).
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