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ANVISA registration 81582089010Active

Guide Wire

ANVISA Registration Number: 81582089010LITORAL COMERCIO DE PRODUTOS MEDICOS E HOSPITALARES LTDA - MESP MEDICAL A/SRisk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
FIO-GUIA DE NITINOL HIDROFÍLICO POSEIDON
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Risk class
Class II
Registration details
Registration Number
81582089010
Process Number
25351179902202232
CNPJ
25164770000109
Company information
Registration Holder
LITORAL COMERCIO DE PRODUTOS MEDICOS E HOSPITALARES LTDA - ME
Manufacturer
SP MEDICAL A/S
Manufacturing Country
Denmark
PT: DINAMARCA
Dates and status
Publication Date
Jul 28, 2022
Status
Active
Official value: VIGENTE
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 81582089010 and manufactured by SP MEDICAL A/S. The registration is held by LITORAL COMERCIO DE PRODUTOS MEDICOS E HOSPITALARES LTDA - ME 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.