853 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AMBU NEUROLINE GROUND
FDA 510(k)
FDA Class 2
·Neurology
T2 HUMERAL NAIL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
POLYMER COATED, POWDER-FREE LATEX EXAMINATION GLOVE WITH PROTEIN LABELLING CLAIM, CONTAINS 50 MICROGRAMS OR LESS OF TOTA
FDA 510(k)
FDA Class 1
·General Hospital
CARELINK
FDA Adverse Event
Malfunction
·RICE CREEK MFG·Product code DXY·April 10, 2013
I-STAT CTNI CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE INC.·Product code MMI·May 23, 2008
SPRINT
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·April 12, 2011
E1 RINGLOC BIPOLAR 28X51MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·August 31, 2016
RINGLOC HIP SYSTEM ACETABULAR BI-POLAR CUP
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code JDI·June 15, 2017
E1 RINGLOC BIPOLAR 28X43MM
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code HBE·June 22, 2016
E1 HI-WALL LINER RINGLOC-X
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·June 2, 2017
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·March 26, 2012
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 13, 2010
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 7, 2010
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 16, 2011
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 23, 2011
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 28, 2011
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·March 27, 2012
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 17, 2012
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 7, 2010
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·October 10, 2010