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ANVISA registration 10324860023Valid until Apr 30, 2027

Guide Wire

ANVISA Registration Number: 10324860023NIPRO MEDICAL LTDANIPRO MEDICAL LTDARisk Class IV
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
FIO GUIA HIDRÓFILO NIPRO AQUALINER
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Risk class
Class IV
Registration details
Registration Number
10324860023
Process Number
25351005662200700
CNPJ
00762455000144
Company information
Registration Holder
NIPRO MEDICAL LTDA
Manufacturer
NIPRO MEDICAL LTDA
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Apr 30, 2007
Validity
30/04/2027
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Guide Wire in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10324860023 and manufactured by NIPRO MEDICAL LTDA. The registration is held by NIPRO MEDICAL LTDA with validity until Apr 30, 2027.

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.