8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OSCOR MEDICAL CORP PERMANENT PACING LEAD
FDA 510(k)
FDA Class 3
·Cardiovascular
Apyx Helium Plasma Generator (APYX-200H/P, APYX-JS3/RS3)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SONOACE 9900 DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
PORTEX® BIVONA® AIRE-CUF® ADULT TRACHEOSTOMY TUBES
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD INC.·Product code JOH·September 1, 2016
PORTEX® BIVONA® AIRE-CUF® ADULT TRACHEOSTOMY TUBES
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD INC.·Product code JOH·September 1, 2016
A HIGH RES SSP UNITRAY W/TAQ10
FDA Adverse Event
Malfunction
·LIFE TECHNOLOGIES·Product code MZI·July 10, 2015
ON-Q PAIN PUMP
FDA Adverse Event
Injury
·I-FLOW LLC·Product code MEB·January 9, 2013
E CYLINDER WITH INTEGRATED FLOW METER
FDA Adverse Event
Malfunction
·LIFE GAS COMPANY·Product code BYJ·September 30, 2010