8 results
·
17ms
·
Sources: EU EUDAMED, US FDA
PINCH SENSOR, MODEL PF001
FDA 510(k)
FDA Class 2
·Orthopedic
ACME MODEL 8500 WHEELCHAIR SCALE
FDA 510(k)
FDA Class 1
·Physical Medicine
NON-STERILE POWDERED LATEX EXAMINATION GLOVES WITH A PROTEIN CLAIM ON LABELING
FDA 510(k)
FDA Class 1
·General Hospital
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·January 4, 2017
ITREL 3
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 14, 2013
UNKNOWN TEDS
FDA Adverse Event
Other
·COVIDIEN·Product code DWL·November 24, 2010
CUSTOM DEFINED PRODUCT
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES DR·Product code DXO·July 3, 2014
STERRAD® NX STERILIZER
FDA Adverse Event
Malfunction
·ADVANCED STERILIZATION PRODUCTS·Product code MLR·February 20, 2018