194 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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COTTONY II, SILKY II POLYDEK & TEVDEK II POLYESTER SUTURE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ROLLO 210X30X12E.PRINTER
FDA UDI
AB MEDICA GROUP, S.A.·08428763005704·
Humeris Shoulder
FDA UDI
FX SOLUTIONS·03701037304556·TRIAL HUMERIS STEM T19
740 SELECT
FDA UDI
ZOE MEDICAL INCORPORATED·00851920007248·The 740 SELECT Monitor is intended for monitori...
COLOR BUFFED (CB) DDH FEMORAL STEM
FDA 510(k)
FDA Class 2
·Orthopedic
TI500 GLOBE-TROTTER TRANSPORT SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
POLARCATH
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SAN JOSE·Product code DQY·March 26, 2013
ATTAIN OTW
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·March 16, 2011
GE OEC 8800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEM INC.·Product code JAA·March 28, 2008
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 16, 2012
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·November 11, 2010
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 23, 2011
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·May 9, 2011
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 18, 2012
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 16, 2012
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 2, 2012
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·October 5, 2010
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·January 10, 2011
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 17, 2011
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·March 2, 2011