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ANVISA registration 10216710398Valid until Aug 23, 2031

CARDIOVASCULAR GUIDE WIRE

ANVISA Registration Number: 10216710398PHILIPS MEDICAL SYSTEMS LTDAVOLCANO CORPORATIONRisk Class IV
Verified
Device names
Technical name
CARDIOVASCULAR GUIDE WIRE
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PT: FIO GUIA CARDIOVASCULAR
Commercial name
Fio-Guia de Pressão OmniWire
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Risk class
Class IV
Registration details
Registration Number
10216710398
Process Number
25351881282202114
CNPJ
58295213000178
Company information
Registration Holder
PHILIPS MEDICAL SYSTEMS LTDA
Manufacturer
VOLCANO CORPORATION
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Aug 23, 2021
Validity
23/08/2031
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 10216710398 and manufactured by VOLCANO CORPORATION. The registration is held by PHILIPS MEDICAL SYSTEMS LTDA with validity until Aug 23, 2031.

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.