10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HEARTSINE SAMARITAN PAD 350P
FDA 510(k)
FDA Class 3
·Cardiovascular
MANTARAY GUIDEWIRES
FDA 510(k)
FDA Class 2
·Cardiovascular
PROFILE 1064 LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BD¿ BULK, NON-STERILE NEEDLE
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·February 7, 2018
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 20, 2025
NEEDLE SPINAL S/SU 25GA 3-1/2IN QUINCKE
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code BSP·March 27, 2019
LIBERTY CYCLER SET, SINGLE CONN./EXT. DL
FDA Adverse Event
Malfunction
·REYNOSA MANUFACTURING·Product code FKX·May 15, 2013
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 27, 2014
INPECO SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT GERMANY·Product code JQP·June 14, 2011
NEEDLE SPINAL S/SU 25GA 3-1/2IN QUINCKE
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code BSP·October 25, 2019