10,000 results
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97ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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TELEFLEX MEDICAL
FDA registration
TELEFLEX MEDICAL·5 products·🇮🇪 Ireland
TELEFLEX MEDICAL
FDA registration
TELEFLEX MEDICAL·3 products·🇮🇪 Ireland
TELEFLEX MEDICAL INTRODUCER CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
TELEFLEX MEDICAL INTRODUCER NEEDLE
FDA 510(k)
FDA Class 1
·Cardiovascular
MODIFIED TELEFLEX MEDICAL INTRODUCER CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
Teleflex Medical Inc.
FDA registration
Teleflex Medical Inc.·4 products·🇺🇸 United States
Teleflex Medical LLC
FDA registration
Teleflex Medical LLC·547 products·🇺🇸 United States
Teleflex Medical LLC
FDA registration
Teleflex Medical LLC·15 products·🇺🇸 United States
Teleflex Medical LLC
FDA registration
Teleflex Medical LLC·2 products·🇺🇸 United States
Teleflex Medical Sdn. Bhd.
FDA registration
Teleflex Medical Sdn. Bhd.·16 products·🇲🇾 Malaysia
Teleflex Medical OEM LLC
FDA registration
Teleflex Medical OEM LLC·8 products·🇺🇸 United States
TELEFLEX MEDICAL
FDA Adverse Event
Injury
·TELEFLEX·Product code CAZ·April 12, 2019
TELEFLEX MEDICAL
FDA Adverse Event
Injury
·TELEFLEX·Product code KNQ·February 11, 2008
TELEFLEX MEDICAL
FDA Adverse Event
Injury
·TELEFLEX MEDICAL·Product code MCW·May 18, 2015
Teleflex Medical de Tecate, S. de R.L de C.V.
FDA registration
Teleflex Medical de Tecate, S. de R.L de C.V.·72 products·🇲🇽 Mexico
Teleflex Medical de Mexico, S. de R.L. de C.V.
FDA registration
Teleflex Medical de Mexico, S. de R.L. de C.V.·127 products·🇲🇽 Mexico
TELEFLEX MEDICAL AORTIC PUNCH, DISP.
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code DWS·December 8, 2009
WECK/TELEFLEX MEDICAL NEEDLE ELECTRODE
FDA Adverse Event
Injury
·WECK/TELEFLEX MEDICAL·Product code GXZ·June 20, 2013
TELEFLEX MEDICALS PILLING WECKSORB NEUROSPONGES
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL LLC·Product code MDM·September 25, 2025
AC3 OPTIMUS IABP TELEFLEX MEDICAL
FDA Adverse Event
Injury
·ARROW INTERNATIONAL, LLC (SUBSIDIARY OF TELEFLEX, INCORPORATED)·Product code DSP·October 12, 2021