2,516 results · 58ms · Sources: EU EUDAMED, 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