2,516 results
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58ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CELLEX
FDA UDI
Therakos LLC·10705030100009·CellEx Instrument
CELLEX
FDA UDI
Therakos LLC·20705030200003·CellEx Procedural Kit
CELLEX
FDA UDI
Therakos LLC·00705030000036·CellEX Procedural Kit RoHS 3 Correct Connect (US)
CELLEX
FDA UDI
Therakos LLC·00705030000029·CellEX Procedural Kit RoHS 3 Correct Connect (OUS)
CELLEX
FDA UDI
Therakos LLC·00705030000012·CellEx Procedural Kit
CELLEX
FDA UDI
Therakos LLC·00705030000050·Cellex Procedural Kit U.S.
CELLEX
FDA UDI
Therakos LLC·00705030000005·CellEx Procedural Kit
CELLEX
FDA UDI
Therakos LLC·20705030300000·CellEx Light Assembly
CELLEX QSARS-COV-2 IGG/IGM RAPID TEST
FDA Adverse Event
Malfunction
·CELLEX·Product code QKO·August 7, 2020
CELLEX PHOTOPHERESIS PROCEDURAL KIT
FDA Adverse Event
Malfunction
·THERAKOS CELLEX·Product code LNR·December 20, 2010
PHOTOPHERESIS PROCEDURAL KIT
FDA Adverse Event
Malfunction
·THERAKOS CELLEX·Product code LNR·December 20, 2010
PHOTOPHERESIS PROCEDURAL KIT; CELLEX KIT
FDA Adverse Event
Malfunction
·THERAKOS CELLEX·Product code LNR·May 30, 2011
KIT, PHOTOPHERESIS PROCEDURAL
FDA Adverse Event
Malfunction
·THERAKOS CELLEX·Product code LNR·May 30, 2011
CELLEX
FDA Adverse Event
Malfunction
·THERAKOS, INC.·Product code LNR·December 1, 2016
CELLEX
FDA Adverse Event
Malfunction
·THERAKOS, INC.·Product code LNR·April 15, 2014
CELLEX
FDA Adverse Event
Malfunction
·THERAKOS, INC.·Product code LNR·October 20, 2014
FLUIDOTHERAPY FT110 SINGLE
FDA Adverse Event
Injury
·DJ ORTHOPEDICS DE MEXICO·Product code LSB·May 24, 2011
CELLEX EXTRACORPOREAL PHOTOPHERESIS SYSTEM
FDA Adverse Event
Malfunction
·MALLINCKRODT PHARMACEUTICALS IRELAND LIMITED·Product code LNR·October 8, 2024
KIT, PHOTOPHERESIS, PROCEDURAL
FDA Adverse Event
Malfunction
·THERAKOS, INC.·Product code LNR·February 28, 2012
CELLEX PROCEDURAL KIT
FDA Adverse Event
Malfunction
·THERAKOS, INC.·Product code LNR·October 30, 2014