HomeBrazilMAGNAMED TECNOLOGIA MEDICA S/A

MAGNAMED TECNOLOGIA MEDICA S/A

Brazil · Sao Paulo
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, Russia — 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
3listed device types
Class I 2Class II 1Class III 0
plus 3 registration records and 1 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
7registered devices
Class II 7
11 including historic records
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
1active registrations
Class 2b 1
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 States3 registration records, 1 510(k), 0 PMA
Brazil7 confirmed, 0 excluded
Manufacturer names merged into this page: MAGNAMED TECNOLOGIA MEDICA S/A · magnamed tecnologia medica s/a

Company information

Country
Brazil
City
Sao Paulo

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

12023 · K221634

FDA listed device types

Set, Tubing And Support, Ventilator (W Harness) 1Tubing, Pressure And Accessories 1Ventilator, Emergency, Powered (Resuscitator) 1

Registration details (sample)

MarketIdentifierNameClass / date
USK221634Oxymag - Transport and Emergency Ventilator2023-05-24
BR80659160002CIRCUITO RESPIRATÓRIOClass II
BR80659160006CIRCUITO RESPIRATÓRIO 2Class II
BR80659160007CIRCUITO RESPIRATÓRIO 3Class II

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