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ANVISA registration 81582089011Active

Guide Wire

ANVISA Registration Number: 81582089011LITORAL 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 PTFE ACCOAT
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Risk class
Class II
Registration details
Registration Number
81582089011
Process Number
25351179957202242
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
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 81582089011 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.