ANVISA registration 10324869001Active

Fistula Needle

Name: Fistula Needle — ANVISA registration 10324869001
Creator: NIPRO MEDICAL LTDA
Keywords: Fistula Needle, Agulha de fístula, AVF SAFETOUCH TULIP NIPRO, 10324869001, Risk Class II, ANVISA registration

ANVISA Registration Number: 10324869001NIPRO MEDICAL LTDANIPRO MEDICAL LTDARisk Class II

Verified

Device names

Technical name: Fistula Needle
Commercial name: AVF SAFETOUCH TULIP NIPRO
Risk class: Class II

Registration details

Registration Number: 10324869001
Process Number: 25351033413202669
CNPJ: 00762455000144

Company information

Registration Holder: NIPRO MEDICAL LTDA
Manufacturer: NIPRO MEDICAL LTDA
Manufacturing Country: Brazil

Dates and status

Publication Date: Mar 09, 2026
Validity: VIGENTE
Last Updated: 08/18/2026 19:00:00

About this record

Access comprehensive regulatory information for Fistula Needle in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10324869001 and manufactured by NIPRO MEDICAL LTDA. The registration is held by NIPRO MEDICAL 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.