755 results · 29ms · Sources: EU EUDAMED, US FDA

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WARMAIR MODEL 135 HYPERTHERMIA SYSTEM (CONTROLLER AND BLANKETS)

FDA 510(k)
FDA Class 2 ·Cardiovascular

LARGE CANNULATED SCREWS

FDA UDI
Smith & Nephew, Inc.·03596010064158·CANNULATED HIP PIN 105MM

PHYSICIAN'S DESKTOP REVIEW

FDA 510(k)
FDA Class 2 ·Radiology

THERMODILUTION CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·August 14, 2015

MYNX CADENCE

FDA Adverse Event
Malfunction ·ACCESSCLOSURE, INC.·Product code MGB·April 19, 2013

CONSERVE(R) TOTAL A-CLASS(R) FEMORAL HEAD

FDA Adverse Event
Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·September 26, 2014

ACS POLY 20D 28 GR3

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·June 2, 2011

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·January 5, 2017

UNKNOWN

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·December 15, 2015

UNKNOWN

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·November 19, 2015

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·June 17, 2016

UNKNOWN

FDA Adverse Event
Injury ·COOK INC·Product code DTK·June 13, 2016

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·November 17, 2016

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·September 27, 2016

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·June 24, 2016

UNKNOWN

FDA Adverse Event
Death ·WILLIAM COOK EUROPE·Product code DTK·June 9, 2016

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·March 1, 2016

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·November 19, 2015

NC QUANTUM APEX

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·April 6, 2026