19 results
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22ms
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Sources: EU EUDAMED, US FDA
GENERATOR, PULSE, BIPOLAR, MODEL #604
FDA 510(k)
FDA Class 3
·Cardiovascular
CoRoent
FDA UDI
Nuvasive, Inc.·00887517809391·Interlock II, 7x17x14mm 15°
BD Prevue II Peripheral Vascular Access System
FDA UDI
Bard Access Systems, Inc.·00801741215049·BD Prevue II Battery
Bard® Urethral Catheterization Tray with Red Rubber Coude Catheter
FDA UDI
C. R. Bard, Inc.·00801741030451·Bard® Urethral Catheterization Tray with Red Ru...
The Orthodontic Store
FDA UDI
Young Innovations, Inc.·00843471184707·.022 U/L Std. Comb. Weld Size#15
BARD® UNIVERSAL CATHETERIZATION TRAY
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code OHR·February 15, 2019
NA
FDA UDI
aap Implantate AG·04042409262227·Handle with quick coupling, with torque limiter...
NASOPORE EAR
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
FLEXIBLE CUTTING SCISSORS
FDA 510(k)
FDA Class 1
·Gastroenterology, Urology
IMED IV PUMP
FDA Adverse Event
Injury
·IMED CORP.·Product code FRN·December 4, 1995
I-STAT ACT CELITE CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JBP·August 23, 2022
I-STAT ACT CELITE CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JBP·August 23, 2022
OPEN SPINE CLAMP DRIVER
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·April 24, 2014
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Injury
·EV3 NEUROVASCULAR·Product code OUT·October 3, 2012
ACCU-CHEK ACTIVE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·September 5, 2007
I-STAT ACT CELITE CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JBP·October 11, 2022
I-STAT ACT CELITE CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JBP·January 11, 2023
I-STAT ACT CELITE CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JBP·January 11, 2023
GE Healthcare, Compact Airway Modules E-CO, E-COV, E-COVX, E-CAiO, E-CAiOV and E-CAiOVX. The Datex-Ohmeda S/5MT Compact Airway Module, E-CAiOVX family is used for monitoring hospital patients respiration, ventilation, and gas exchange status.
FDA Enforcement
Class II
·Terminated·GE Healthcare, LLC·June 25, 2014