95 results
·
29ms
·
Sources: EU EUDAMED, US FDA
DIACAP LO PS (10, 12, 15) AND DIACAP HI PS (10, 12, 15, 18, 20) HEMODIALYZERS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SOLIDEA
FDA UDI
CALZIFICIO PINELLI SRL·08300496071518·STRIPE GAME PERSEO, SIZE S, NERO, GRADUATED COM...
GRADIA
FDA 510(k)
FDA Class 2
·Dental
VITALSAT SERIES
FDA 510(k)
FDA Class 2
·Cardiovascular
WAVEWRITER ALPHA PRIME 16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 14, 2022
S5 ROLLER PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 26, 2012
S5 ROLLER PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012
S5 ROLLER PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012
S5 SYSTEM
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010
S5 ROLLER PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012
S5 ROLLER PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012
S5 SYSTEM
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010
S5 SYSTEM
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010
S5 SYSTEM
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010
PROXIMATE PPH PROCEDURE SET
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·April 22, 2013
SELF CENT HIP 53X28 BLU
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWY·April 15, 2011
ASCENSIA BREEZE2
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE LLC·Product code NBW·July 3, 2008
S5 SENSOR MODULE FOR BUBBLE DETECTOR
FDA Adverse Event
Malfunction
·SORIN GROUP DEUTSCHLAND·Product code DTW·October 21, 2016
LCD TOUCHSCREEN, RP150, S5
FDA Adverse Event
Malfunction
·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 14, 2012
LCD TOUCHSCREEN, RP150, S5
FDA Adverse Event
Malfunction
·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 15, 2012