3,292 results · 24ms · Sources: EU EUDAMED, US FDA

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MEDRAD® 1.5T eCoil Interface Device (for Siemens)

FDA UDI
BAYER MEDICAL CARE INC.·00616258009056·"ASSY,COIL,SIEMENS SYMPHONY FID,MC (60727528)"

DxTx Medical 1.5T Imaging Device (for Siemens)

FDA UDI
DXTX MEDICAL INC·00850011472200·Ecoil ID - FID SYM

MEDRAD® 1.5T eCoil Interface Device (for Siemens)

FDA UDI
BAYER MEDICAL CARE INC.·00616258009049·"ENDO INTERFACE DEVICE SIEMENS 1.5T SYM (607278...

DxTx Medical 1.5T eCoil Imaging Device (for Siemens)

FDA UDI
DXTX MEDICAL INC·00850011472217·Ecoil ID - FID SYM FRU

SHIMADZU GAS CHROMATOGRAPHY

FDA Adverse Event
Malfunction ·SHIMADZU U.S.A. MANUFACTURING, INC.·Product code DOP·June 21, 2023

GCMS -QP2020 CL,GCMS-TQ8050 CL

FDA Adverse Event
Malfunction ·SHIMADZU COPORATION·Product code DOP·August 1, 2023

ORTHO SUMMIT SAMPLE HANDLING SYSTEM

FDA Adverse Event
Other ·HAMILTON BONADUZ AG·Product code JTC·April 10, 2006

ORTHO SUMMIT SAMPLE HANDLING SYSTEM

FDA Adverse Event
Other ·HAMILTON BONADUZ AG·Product code JTC·April 10, 2006

ORTHO SUMMIT SAMPLE HANDLING SYSTEM

FDA Adverse Event
Other ·HAMILTON BONADUZ AG·Product code JTC·April 10, 2006

GE OEC 9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·December 30, 2008

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·December 30, 2020

HOLDING+DISTRACTION INSTR F/ECD

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code FZX·June 23, 2023

COATED VICRYL

FDA Adverse Event
ETHICON, INC.·Product code GAW·April 10, 2018

PAR, RIGHT, W/TRIDENT SIZE F ID

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·November 13, 2018

PAR IMPLANT, RIGHT, TRIDENT SIZE F ID

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·July 11, 2017

CS BED 9153650455

FDA Adverse Event
Malfunction ·INVACARE CONTINUING CARE·Product code FNL·June 4, 2015

HUDSON AQUATHERM III, ELECTRONIC HEATER

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code BTT·August 14, 2014

SET, EXTENSION BLOODLINE FOR CRRT 36 IN CUSTOM

FDA Adverse Event
Malfunction ·MOLDED PRODUCTS, INC.·Product code FID·June 11, 2012

FRESENIUS USA

FDA Adverse Event
Death ·FRESENIUS USA·Product code FID·April 10, 2003

VENOUS HANSON LINE

FDA Adverse Event
Malfunction ·Product code FID·March 13, 2019