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ANVISA registration 81576620044Valid until May 19, 2035

CARDIOVASCULAR GUIDE WIRE

ANVISA Registration Number: 81576620044CORDIS MEDICAL BRASIL LTDACORDIS US CORP.Risk Class IV
Verified
Device names
Technical name
CARDIOVASCULAR GUIDE WIRE
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PT: FIO GUIA CARDIOVASCULAR
Commercial name
FIO GUIA CORDIS EMERALD
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Risk class
Class IV
Registration details
Registration Number
81576620044
Process Number
25351377563202410
CNPJ
27548227000122
Company information
Registration Holder
CORDIS MEDICAL BRASIL LTDA
Manufacturer
CORDIS US CORP.
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
May 19, 2025
Validity
19/05/2035
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for CARDIOVASCULAR 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 81576620044 and manufactured by CORDIS US CORP.. The registration is held by CORDIS MEDICAL BRASIL LTDA with validity until May 19, 2035.

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.