HomeFrancePhilips France

Philips France

France · Paris
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Canada, Australia — 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
7listed device types
Class I 0Class II 7Class III 0
plus 8 registration records and 1 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
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
1 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
IIb 1
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 States8 registration records, 1 510(k), 0 PMA, 103 excluded
Brazil0 confirmed, 21 excluded
Saudi Arabia0 confirmed, 14 excluded
Canada0 confirmed, 29 excluded
Manufacturer names merged into this page: Philips France · PHILIPS FRANCE

Company information

Country
France
City
Paris

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

12025 · K250569

FDA listed device types

System, Measurement, Blood-Pressure, Non-Invasive 1Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) 1Electrocardiograph 1Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase 1Oximeter 1Computer, Diagnostic, Programmable 1Continuous Measurement Thermometer 1

Registration details (sample)

MarketIdentifierNameClass / date
USK250569Cardiologs Holter Platform2025-08-06

Similar companies

@bloc SAS
France · markets 0
A. Legrand SAS
France · markets 0
Acime Frame SAS
France · markets 5
ADDEV Materials SAS
France · markets 1
ADHEX TECHNOLOGIES SAS
France · markets 5
Advanced Silicone Coating SAS
France · markets 0
Is this your company? Claim the page, add information or report a data error.Claim / report an error →