25 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SEAL-AWAY CS INTRODUCER KIT, MODELS 407514, 407515
FDA 510(k)
FDA Class 2
·Cardiovascular
Diamond D
FDA UDI
Keystone Industries·H66810130291·Denture Acrylic HC Lrp pwd
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033588529·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033588536·
Matira
FDA UDI
Kalitec Direct LLC·B073DRK010029·Drill Guide, Variable, Attached Handle
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033588550·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033588543·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033588574·
Cosmolock
FDA UDI
Kalitec Direct LLC·B07310K0100290·Caddie Lid, MIS Rods and Caps
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033588567·
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0130201·PLATE CALIPER
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 18, 2021
HOME HEALTH MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
INFUSOMAT P
FDA 510(k)
FDA Class 2
·General Hospital
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·January 27, 2012
TSRH SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code MNI·April 16, 2013
ACIST
FDA Adverse Event
Malfunction
·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·August 1, 2013
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·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
2250051-2008-00107
FDA Adverse Event
Malfunction
·Product code JTC·February 26, 2008