29 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BIOCHECK HUMAN CARDIAC TROPONIN-I IMMUNOASSAY TEST KIT
FDA 510(k)
FDA Class 2
·Clinical Chemistry
SureFlex
FDA UDI
AMERICAN MEDICAL SYSTEMS·00878953000183·550 µm Lithotripsy Fiber
Diamond D
FDA UDI
Keystone Industries·H66810130621·Denture Acrylic HC Light 1 lb P& L
Dornier MedTech
FDA UDI
DORNIER MEDTECH AMERICA, INC.·04049958003097·270 micron Holmium Laser Fiber Cable, Single Us...
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033454244·
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0130120·Segmental Rod Reducer Driver
STYROFOAM CUTTERS FOR BLOCK CASTING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
BACTEC MGIT 960 SIR KITS
FDA 510(k)
FDA Class 2
·Microbiology
50-13062 DEKALB VASCULAR PACK
FDA Adverse Event
Malfunction
·DEROYAL INDUSTRIES, INC.·Product code KDD·June 17, 2002
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
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 1, 2013
CAPSUREEPI
FDA Adverse Event
Injury
·MPRI·Product code DTB·August 15, 2014