24 results
·
22ms
·
Sources: EU EUDAMED, US FDA
KONICA LASER IMAGER, DRYPRO MODEL 751/752
FDA 510(k)
FDA Class 2
·Radiology
Diamond D
FDA UDI
Keystone Industries·H66810130521·Denture Acrylic SC Orig Pwd
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450409183·
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0130120·Segmental Rod Reducer Driver
InTess C Cervical Cage System
FDA UDI
Kalitec Direct LLC·B07309K01305N0·Cervical Rasp, 14 x 11, 5mm, 0 Degree, No Taper
NUMED TYSHAK II AND Z-MED II PTV CATHETERS
FDA 510(k)
FDA Class 2
·Cardiovascular
RESPIRONICS BILICHEK NON-INVASIVE-100-0800-20; BILIRUBIN ANALYZER
FDA 510(k)
FDA Class 1
·Clinical Chemistry
SCHILLER
FDA Adverse Event
Malfunction
·SCHILLER AG·Product code MHX·November 2, 2006
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 17, 2017
DISC LT DSTL HMRL BDY SET
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDC·April 1, 2019
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 17, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 19, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 19, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 17, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Death
·BIOMET UK LTD.·Product code JDC·May 19, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 19, 2017
6800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 1, 2013
ACCU-CHEK FLEXLINK PLUS
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code FRN·March 4, 2011
IN SITU BENDER-RIGHT
FDA Adverse Event
Malfunction
·SYNTHES TUTTLINGEN·Product code HXP·August 15, 2014
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 17, 2017