748 results · 22ms · Sources: EU EUDAMED, US FDA

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TURON RSP SOCKET SHELL-NEUTRAL MODEL 508-02-000, TURON RSP SOCKET SHELL-OFFSET MODEL 508-02-001

FDA 510(k)
FDA Class 2 ·Orthopedic

JOBST Anti-Em

FDA UDI
BSN MEDICAL, INC.·00035664116293·ANTI-EMB STOCKINGS WAIST HIGH LARGE REGULAR WHI...

DONJOY

FDA UDI
DJO, LLC·00888912018043·ICEMAN CLEARCUBE W/UNIV COLD PAD, S, RH

MicroSelectron Digital

FDA UDI
Nucletron B.V.·08717213026322·microSelectron Transfer Tube for 6F Flexibles (19)

DONJOY

FDA UDI
DJO, LLC·00190446738336·ICEMAN CLEAR3 W/ UNIVERSAL COLD PAD, S, RH, ORT...

FIL 1520

FDA 510(k)
FDA Class 2 ·Anesthesiology

RESMART CPAP, RESMART AUTO-CPAP AND RESMART HUMIDIFIER

FDA 510(k)
FDA Class 2 ·Anesthesiology

UNKNOWN

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

TRILOGY 100

FDA Adverse Event
Malfunction ·RESPIRONICS INC.·Product code CBK·May 6, 2013

COAGUCHEK ® XS SYSTEM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·June 2, 2011

WALLFEX ENTERAL COLONIC STENT

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC·Product code MQR·August 13, 2008

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