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