8 results
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25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ULTRASOUND TRANSDUCER DRAPE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
AUTODELFIA NEONATAL IRT L KIT, MODEL B022-112
FDA 510(k)
FDA Class 2
·Clinical Chemistry
HV Screw System
FDA 510(k)
FDA Class 2
·Orthopedic
LD304 MATERNITY BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code HDD·May 29, 2015
DEVILBISS
FDA Adverse Event
Injury
·SUNRISE MEDICAL HHG, INC.·Product code CAF·November 8, 2001
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 21, 2013
COOL CAP
FDA Adverse Event
NATUS MEDICAL·Product code MXM·January 14, 2011
LEAD, UNKNOWN
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code MHY·July 31, 2014