9 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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WRIST AUTOMATIC BLOOD PRESSURE MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
MARINA MEDICAL SILICONE PESSARY
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
VALEO VT-601 SERIES IR THERMOMETER
FDA 510(k)
FDA Class 2
·General Hospital
RELOAD FOR 60MM ECHELON
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·October 22, 2021
OT VERIO2 METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 8, 2016
WAVEWRITER ALPHA? 16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·January 20, 2026
THERMOPHORE AUTOMATIC MOIST HEAT PACK
FDA Adverse Event
Malfunction
·BATTLE CREEK EQUIPMENT COMPANY·Product code IRT·February 25, 2013
ASKU
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA INC.·Product code DTE·June 16, 2011
ECHO
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·August 25, 2008