HomeBrazilCANON MEDICAL SYSTEMS DO BRASIL LTDA

CANON MEDICAL SYSTEMS DO BRASIL LTDA

Brazil
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, Canada — 3 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
97510(k) clearances
Class I 0Class II 0Class III 0
plus 0 registration records and 97 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
2registered devices
Class II 2
8 including historic records
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
19active device licences
Class II 11Class III 8
58 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States0 registration records, 97 510(k), 0 PMA, 18 excluded
Brazil2 confirmed, 5 excluded
Saudi Arabia0 confirmed, 2 excluded
Canada19 confirmed, 6 excluded
Manufacturer names merged into this page: CANON MEDICAL SYSTEMS CORPORATION · CANON MEDICAL SYSTEMS DO BRASIL LTDA

Company information

Country
Brazil

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

152018
102019
152020
152021
102022
102023
82024
92025
52026

Registration details (sample)

MarketIdentifierNameClass / date
USK253596Aquilion ONE (TSX-308A/TSX-306A) V2.02026-05-20
USK253625Vantage Fortian/Orian 1.5T, MRT-1550, V10.0 with AiCE Reconstruction Processing Unit for MR2026-03-27
USK260078Aquilion ServeSP (TSX-307B) V2.02026-03-13
BR10295030057SISTEMA DE DIAGNÓSTICO POR ULTRASSOMClass II
BR10295030066RESSONÂNCIA MAGNÉTICAClass II
CA64883INFINIX VB-IClass III
CA64888INFINIX CS-IClass III
CA64890INFINIX VS-IClass III

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