13 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CLEARVIEW BLOWER/MISTER
FDA 510(k)
FDA Class 2
·General Hospital
VISTAKON (NARAFILCON) A SOFT CONTACT LENS
FDA 510(k)
FDA Class 2
·Ophthalmic
Amsco Evolution Medium Steam Sterilizer
FDA 510(k)
FDA Class 2
·General Hospital
BD FACSCALIBUR¿ FLOW CYTOMETER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·January 31, 2023
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Injury
·ANIMAS CORPORATION·Product code LZG·February 22, 2013
ASR ACETABULAR IMPLANT 48?
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 7, 2011
PRESEP CENTRAL VENOUS OXIMETRY SET
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES, PR·Product code DQE·August 1, 2014
BD FACSCALIBUR FLOW CYTOMETER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·March 31, 2023
BD FACSCALIBUR¿ FLOW CYTOMETER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·March 31, 2023
BD FACSCALIBUR¿ FLOW CYTOMETER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·January 20, 2023
BD FACSCALIBUR¿ FLOW CYTOMETER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·July 24, 2023
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·April 14, 2015
UNK
FDA Adverse Event
Injury
·VISTAKON·Product code LPL·October 11, 2010