31 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Infrared Thermometer
FDA 510(k)
FDA Class 2
·General Hospital
Blade Handle
FDA UDI
KATENA PRODUCTS, INC.·00841668112366·CHUCK HANDLE #3K 10CM LONG
Blade Handle
FDA UDI
KATENA PRODUCTS, INC.·00841668112373·CHUCK HANDLE #3KA 7.5CM LONG
Blade Handle
FDA UDI
KATENA PRODUCTS, INC.·00841668112380·BARD-PARKER HANDLE #3
BD INTEGRA¿ SYRINGE WITH NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code MEG·November 27, 2017
HIP MODULE FOR THE STEALTHSTATION SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
ASPECT MEDICAL SYSTEMS PEDIATRIC BIS EEG SENSOR, MODEL 186-0110
FDA 510(k)
FDA Class 2
·Neurology
BD INTEGRA¿ SYRINGE WITH DETACHABLE NEEDLE
FDA Adverse Event
Injury
·BECTON DICKINSON MEDICAL SYSTEMS·Product code MEG·June 1, 2018
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 29, 2025
ELUVIATM DRUG-ELUTING VASCULAR STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NIU·January 28, 2019
SMARTSET GHV GENTAMICIN 40G
FDA Adverse Event
Injury
·9610921 DEPUY CMW·Product code LOD·October 27, 2014
MEDTRONIC O-ARM
FDA Adverse Event
Malfunction
·MEDTRONIC·Product code IZL·August 3, 2011
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·July 2, 2013
ARCHITECT C16000 SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code JJE·June 25, 2012
PIPELINE
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·March 17, 2020
PIPELINE
FDA Adverse Event
Death
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·March 17, 2020
AORTIC EXCLUDER AAA ENDOPROSTHESIS (C3)
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·July 25, 2019
UNK - SCREWS: TRAUMA
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·July 30, 2019
ARCHITECT C16000
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code JJE·May 10, 2021
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAM·April 16, 2020