471 results
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44ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Matrx PB Deep Heavy-Duty Back Cover
FDA UDI
Motion Concepts Inc·07540147000639·Matrx Posture Back (PB) Deep Heavy-Duty Back Co...
DDC TECHNOLOGIES, INC.
FDA registration
DDC TECHNOLOGIES, INC.·1 product·🇺🇸 United States
AL-40
FDA UDI
DDC TECHNOLOGIES, INC.·00860002307022·Pulsed Alexandrite Laser
EPY-50
FDA UDI
DDC TECHNOLOGIES, INC.·00860002307039·Pulsed Nd:YAG Laser
Polylase
FDA UDI
DDC TECHNOLOGIES, INC.·00860002307046·Dual Output Pulsed Alexandrite and Nd:YAG Laser
Polylase
FDA UDI
DDC TECHNOLOGIES, INC.·90860002307018·Pulsed Alexandrite Laser
Polylase
FDA UDI
DDC TECHNOLOGIES, INC.·00860002307008·Dual Output Pulsed Alexandrite and Nd:YAG Laser
ATL
FDA UDI
Advanced Technology Laser Co.,Ltd.·06970507240022·
PENUMBRA DDC CATHETERS
FDA 510(k)
FDA Class 2
·Cardiovascular
DIOX-602
FDA UDI
DigiMed Co., Ltd.·08800021800014·The DIOX-602 is a hand-held diagnostic dental x...
Welch Allyn, Inc.
FDA UDI
WELCH ALLYN, INC.·00732094265873·ELI280 12-Lead Multi-Channel Electrocardiograph...
Welch Allyn, Inc.
FDA UDI
WELCH ALLYN, INC.·00732094265866·ELI280 12-Lead Multi-Channel Electrocardiograph...
Welch Allyn, Inc.
FDA UDI
WELCH ALLYN, INC.·00732094265859·ELI280 12-Lead Multi-Channel Electrocardiograph...
THORATEC VENTRICULAR ASSIST DEVICE SYSTEM (DDC)
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·November 7, 2013
THORATEC VENTRICULAR ASSIST DEVICE SYSTEM (DDC)
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·November 7, 2013
PENUMBRA 5MAX DDC DISTAL DELIVERY CATHETERS
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code NRY·February 9, 2018
VENTRICULAR ASSIST DEVICE (VAD) SYSTEM
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·September 23, 2003
TLC-II DRIVER
FDA Adverse Event
Malfunction
·THORATEC CORPORATION·Product code DSQ·May 30, 2019
THORATEC VENTRICULAR ASSIST DEVICE SYSTEM (DDC)
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·July 13, 2011
THORATEC VENTRICULAR ASSIST DEVICE 9VAD) SYSTEM
FDA Adverse Event
Malfunction
·THORATEC CORP.·Product code DSQ·June 9, 2004