853 results · 24ms · Sources: EU EUDAMED, 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