84 results · 20ms · Sources: EU EUDAMED, US FDA

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QUICKIE 2 WHEELCHAIR

FDA Adverse Event
Malfunction ·QUICKIE DESIGNS INC.·Product code IOR·November 19, 1996

ANSPACH X MAZ

FDA Adverse Event
Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code ERL·October 17, 2014

MEZ BREATHE ATOMIZER

FDA Adverse Event
Malfunction ·HEALTH & LIFE (SUZHOU) CO., LTD.·Product code CCQ·November 5, 2013

TEEX/8-3 MHZ

FDA Adverse Event
Malfunction ·SONOSITE,INC.·Product code IYO·January 11, 2012

OAS 450 MHZ SERVER

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JQP·November 24, 2003

SONICATH 3.2F, 20 MHZ

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORP.·Product code ITX·June 20, 2007

OAS 400 MHZ WORKSTATION

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JTC·March 13, 2003

ACCELERATOR APS CENTRIFUGE MODULE

FDA Adverse Event
Malfunction ·ABBOTT MANUFACTURING INC·Product code JQP·February 18, 2014

LAP/12-5 MHZ TRANSDUCER

FDA Adverse Event
Malfunction ·SONOSITE,INC.·Product code ITX·February 23, 2007

TEE/8-3 MHZ TRANSDUCER

FDA Adverse Event
Malfunction ·SONOSITE, INC.·Product code IYO·February 17, 2009

TEE/8-3 MHZ TRANSDUCER

FDA Adverse Event
Malfunction ·SONOSITE, INC.·Product code IYO·September 12, 2008

TEE/8-3 MHZ TRANSDUCER

FDA Adverse Event
Malfunction ·SONOSITE, INC.·Product code IYO·September 12, 2008

91341 TELEMETRY TRANSMITTER, 1400 MHZ

FDA Adverse Event
Malfunction ·SPACELABS HEALTHCARE·Product code DSI·August 22, 2008

TEE/8-3 MHZ TRANSDUCER

FDA Adverse Event
Malfunction ·SONOSITE, INC.·Product code IYO·August 22, 2008

91341 TELEMETRY TRANSMITTER, 1400 MHZ

FDA Adverse Event
Malfunction ·SPACELABS HEALTHCARE·Product code DSI·August 22, 2008

91341 TELEMETRY TRANSMITTER, 1400 MHZ

FDA Adverse Event
Malfunction ·SPACELABS HEALTHCARE·Product code DRG·August 22, 2008

TEE/8-3 MHZ TRANSDUCER

FDA Adverse Event
Malfunction ·SONOSITE, INC.·Product code IYO·August 29, 2008

TEE/8-3 MHZ TRANSDUCER

FDA Adverse Event
Malfunction ·SONOSITE,INC.·Product code IYO·September 12, 2008

SONICATH ULTRA 3.2F 20 MHZ

FDA Adverse Event
Malfunction ·SCIMED, A DIVISION OF BOSTON SCIENTIFIC CORP·Product code DQO·September 14, 2006

SONICATH ULTRA 3.2F 20 MHZ

FDA Adverse Event
Malfunction ·SCIMED, A DIVISION OF BOSTON SCIENTIFIC CORP·Product code DQO·September 14, 2006