12 results
·
23ms
·
Sources: EU EUDAMED, US FDA
TrachCuff Cuff Controller
FDA 510(k)
FDA Class 2
·Anesthesiology
Premature Babies Micro Vascular Clamp #3
FDA UDI
Geister Medizintechnik GmbH·04057034058022·Premature Babies Micro Vascular Clamp #3
MODIFICATION TO FOX PTA CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
SYNTHES VA LCP ANKLE TRAUMA SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
I-STAT EC8+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code CHL·October 27, 2022
ONE TOUCH ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code NBW·October 30, 2008
ENDOPLEGE CORONARY SINUS CATHETER
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES·Product code DWF·August 23, 2011
ACCU-CHEK SPIRIT COMBO
FDA Adverse Event
Malfunction
·ROCHE HEALTH SOLUTIONS INC·Product code LZG·July 11, 2013
2.7MM VA-LCP LATERAL DISTAL FIBULA PLATE/4 HOLES/LEFT
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HRS·October 11, 2018
BD CATHENA¿ SAFETY IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·July 7, 2022
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·August 12, 2016
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·October 1, 2015