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ANVISA registration 10210419009Active

Guide Wire

ANVISA Registration Number: 10210419009BIOASSIST COMERCIAL LTDAORTUS MEDI-TECH CO., LTDRisk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
FIO GUIA TEFLONADO
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Risk class
Class II
Registration details
Registration Number
10210419009
Process Number
25351414361202113
CNPJ
40334484000120
Company information
Registration Holder
BIOASSIST COMERCIAL LTDA
Manufacturer
ORTUS MEDI-TECH CO., LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Oct 07, 2021
Validity
VIGENTE
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 II medical device is registered under ANVISA number 10210419009 and manufactured by ORTUS MEDI-TECH CO., LTD. The registration is held by BIOASSIST COMERCIAL 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.