Pure Global AI
ANVISA registration 80202919025Active

PERIPHERAL ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 80202919025TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDANEXSTEP MEDICALRisk Class II
Device names
Technical name
PERIPHERAL ANGIOPLASTY BALLOON CATHETER
PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Commercial name
Cateter Balão de Dilatação para PTA All’InCath 035M
Risk class
Class II
Registration details
Registration Number
80202919025
Process Number
25351210292202502
CNPJ
05638301000169
Company information
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).

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.