21 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CoSense ETCO Monitor
FDA 510(k)
FDA Class 2
·Anesthesiology
POUR-PLUS
FDA UDI
Denplus Inc·D8451151107·POUR-PLUS, MDP, 454 g
Neoloy®
FDA UDI
Dentsply International Inc.·D001N1511070·
PEAK MEDICAL
FDA UDI
Peak Medical Distribution Inc.·G45333241511070·9/16 SIZE GREENBERG RETRACTION BLADE
TALOS®-C HA
FDA UDI
MEDITECH SPINE, LLC·B167521511070·
ONYX II FINGER PULSE OXIMETER, MODEL 9550
FDA 510(k)
FDA Class 2
·Cardiovascular
SUPER PORCELAIN EX-3 UNIVERSAL OPAQUE
FDA 510(k)
FDA Class 2
·Dental
NUCLEUS CI522 COCHLEAR IMPLANT WITH SLIM STRAIGHT ELECTRODE
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code MCM·August 22, 2019
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007433·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
BELLAFILL DERMAL FILLER
FDA Adverse Event
Injury
·SUNEVA MEDICAL, INC.·Product code LMH·August 22, 2019
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007471·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007488·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007464·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007440·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007457·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
VENTED HUMIDIFICATION CHAMBER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·June 8, 2016
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013
AUGMENTED INSERT
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 30, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·September 9, 2008
INFANT DUAL HEATED EVAQUA2 BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BZE·October 19, 2016