1,314 results
·
52ms
·
Sources: EU EUDAMED, US FDA
Teleflex Medical Inc.
FDA registration
Teleflex Medical Inc.·4 products·🇺🇸 United States
EXACTA
FDA Adverse Event
Malfunction
·THOMAS MEDICAL PRODUCTS INC.·Product code DYB·July 22, 1998
SM OR-DR. YEH PACK-LF
FDA Adverse Event
Injury
·MEDLINE INDUSTRIES, LP·Product code LRO·August 18, 2025
ARROW SUPER ARROW FLEX 7 FR INTRODUCER SHEATH
FDA Adverse Event
Injury
·TELEFLEX·Product code DYB·March 5, 2020
ARROWGUARD BLUE
FDA Adverse Event
Malfunction
·TELEFLEX INC.·Product code DQO·May 21, 2014
ARROW INTRA AORTIC BALLOON CATHETER 40CC/8FR.
FDA Adverse Event
Malfunction
·TELEFLEX, INC·Product code DSP·October 4, 2012
AGB
FDA Adverse Event
Malfunction
·TELEFLEX, INC·Product code DQO·December 5, 2012
TWO-LUMEN CENTRAL VENOUS CATHETERIZATION KIT WITH BLUE FLEXTIP, ARROWG+ARD BLUE
FDA Adverse Event
Malfunction
·TELEFLEX INC.·Product code DQY·May 9, 2012
ARROWGARD BLUE PLUS QUAD-LUMEN CVC
FDA Adverse Event
Malfunction
·TELEFLEX INC,·Product code FOZ·May 1, 2012
HUDSON RCI
FDA Adverse Event
Malfunction
·TELEFLEX, INC.·Product code BTT·June 14, 2024
LMA UNIQUE
FDA Adverse Event
Malfunction
·TELEFLEX INC.·Product code CAE·October 24, 2017
FLEXTIP PLUS
FDA Adverse Event
Malfunction
·TELEFLEX, INC·Product code OGE·February 20, 2013
PEEL AWAY & SPLIT SHEATH PERCU CATH INTRODUCER
FDA Adverse Event
Injury
·TELEFLEX, INC.·Product code DYB·December 14, 2009
RUSCH
FDA Adverse Event
Malfunction
·TELEFLEX, INC.·Product code KOD·May 11, 2013
ARROW BALLOON WEDGE PRESSURE CATHETER
FDA Adverse Event
Malfunction
·TELEFLEX, INC.·Product code DYG·June 3, 2013
MONODEK SUTURE BN
FDA Adverse Event
Malfunction
·TELEFLEX INC.·Product code NEW·August 26, 2011
ARROW RADIAL ARTERY CATHETERIZATION SET
FDA Adverse Event
Malfunction
·TELEFLEX INC.·Product code DQY·May 10, 2013
RUSCH PEDIATRIC FOLEY CATHETER
FDA Adverse Event
Malfunction
·TELEFLEX, INC.·Product code KOD·June 7, 2013
WECK DISPOSABLE IMA/ENT 3/4" NEEDLE ELECTRODE STERILE ELECTROSURGICAL ELECTRODE
FDA Adverse Event
Malfunction
·TELEFLEX, INC.·Product code HGI·June 14, 2024
PLEUR-EVAC
FDA Adverse Event
Malfunction
·TELEFLEX, INC.·Product code CAC·May 21, 2024