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Home›Brazil›AMERICAN INSTRUMENTS LTDA - EPP

AMERICAN INSTRUMENTS LTDA - EPP

Brazil
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Brazil — 2 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
1510(k) clearances
Class I 0Class II 0Class III 0
plus 0 registration records and 1 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
63registered devices
Class I 15Class II 48
this export covers Class I / II only (the cadastro route)
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
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, 1 510(k), 0 PMA, 287 excluded
Brazil63 confirmed, 10 excluded
Saudi Arabia0 confirmed, 4 excluded
Canada0 confirmed, 20 excluded
Manufacturer names merged into this page: AMERICAN INSTRUMENTS LTDA - EPP

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

11980 · K802379

Registration details (sample)

MarketIdentifierNameClass / date
USK802379HEM-O-SCAN OXYGEN EQUIL. CURVE ANALYZER1980-10-31
BR80251140030EXTENSÃO FLEXÍVELClass II
BR80251140050SAFE BAGClass II
BR80251149010UNIDADE REGULADORA DO MOTOR SMART (URM SMART)Class II

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