22 results
·
18ms
·
Sources: EU EUDAMED, US FDA
MODIFICATION TO ACCESS CEA REAGENTS FOR USE ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 33200, 33205, 33209, 33206
FDA 510(k)
FDA Class 2
·Immunology
FORTRESS COMMUTER FT (FOLDING TRANSPORT)
FDA 510(k)
FDA Class 2
·Physical Medicine
CENTRIA INSULIN RIA
FDA 510(k)
FDA Class 1
·Clinical Chemistry
MICROTAINER SST GOLD
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·June 7, 2018
BD MICROTAINER® EDTA LAVENDAR TUBES
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·May 1, 2018
BD MICROTAINER® EDTA LAVENDAR TUBES
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·May 16, 2018
MICROTAINER SST GOLD
FDA Adverse Event
Malfunction
·BECTON DICKINSON CARIBE LTD·Product code JKA·May 7, 2018
BD MICROTAINER® EDTA LAVENDER TUBES
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·April 27, 2018
BD MICROTAINER® EDTA LAVENDAR TUBES
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·May 3, 2018
BD MICROTAINER® BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·December 3, 2017
PROFEMUR(R) TL STEM
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·March 6, 2013
CONCERTO CRT-D DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014
ADAPTA DR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code NVZ·February 15, 2011
UNKNOWN SPIRALOK ANCHOR
FDA Adverse Event
Injury
·DEPUY MITEK·Product code MBI·June 21, 2007
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017