2,349 results
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53ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Philips France
FDA registration
Philips France·5 products·🇫🇷 France
PHILIPS FRANCE
FDA registration
PHILIPS FRANCE·2 products·🇫🇷 France
Cardiologs Platform
FDA UDI
PHILIPS FRANCE·00884838131958·
Cardiologs Platform
FDA UDI
PHILIPS FRANCE·G637CEA0·
PHILIPS FR/FR2/FR2+ Adult Electrode Pads
FDA UDI
PHILIPS ELECTRONICS NORTH AMERICA CORPORATION·00884838029569·5-pack HS FR/FR2 Defib Pads (DP2/DP6)
PHILIPS FR/FR2/FR2+ Adult Electrode Pads
FDA UDI
PHILIPS ELECTRONICS NORTH AMERICA CORPORATION·00884838023727·HeartStart DP Pads, 5 sets
CARDIOLOGS PLATFORM V2.4.7
FDA Adverse Event
Injury
·PHILIPS FRANCE·Product code DPS·October 3, 2025
CARDIOLOGS PLATFORM - V2.4.10A
FDA Adverse Event
Injury
·PHILIPS FRANCE·Product code DPS·July 1, 2025
CARDIOLOGS PLATFORM - V2.4.10A
FDA Adverse Event
Injury
·PHILIPS FRANCE COMMERICAL·Product code DPS·August 8, 2025
CARDIOLOGS PLATFORM - V 2.4.8A
FDA Adverse Event
Death
·PHILIPS FRANCE COMMERICAL·Product code DPS·October 7, 2025
CARDIOLOGS PLATFORM V2.3.13
FDA Adverse Event
Death
·PHILIPS FRANCE COMMERICAL·Product code DPS·October 21, 2025
CARDIOLOGS PLATFORM V2.3.13
FDA Adverse Event
Death
·PHILIPS FRANCE COMMERICAL·Product code DPS·October 21, 2025
CARDIOLOGS HOLTER PLATFORM
FDA Adverse Event
Death
·PHILIPS FRANCE COMMERICAL·Product code DPS·April 17, 2023
CARDIOLOGS PLATFORM, VERISON 2.4.3
FDA Adverse Event
Injury
·PHILIPS FRANCE COMMERICAL·Product code DPS·May 5, 2025
TEMPUS PRO, BT HEADSET DOCK
FDA Adverse Event
Malfunction
·REMOTE DIAGNOSTIC TECHNOLOGIES LTD.·Product code MHX·September 24, 2025
ALLURA XPER FD10
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code IZI·April 18, 2017
TEMPUS PRO
FDA Adverse Event
Malfunction
·REMOTE DIAGNOSTIC TECHNOLOGIES LTD.·Product code MHX·January 30, 2024
ANGIOSCULPT EVO RX PTCA
FDA Adverse Event
Injury
·PHILIPS IMAGE GUIDED THERAPY CORPORATION·Product code NWX·July 22, 2023
LUMIGUIDE NAVIGATION WIRE 3D ULTRA
FDA Adverse Event
Injury
·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code DQX·February 16, 2026
SKINTACT
FDA Adverse Event
Malfunction
·LEONHARD LANG GMBH·Product code MKJ·June 19, 2019