67 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Emory Cardiac Toolbox 4.3
FDA 510(k)
FDA Class 2
·Radiology
Microline Surgical, Inc
FDA registration
Microline Surgical, Inc·6 products·🇺🇸 United States
Prime Medical LLC
FDA UDI
Prime Medical LLC·00850055249271·PrimePadPlus-K12-3422
Prime Medical LLC
FDA UDI
Prime Medical LLC·00850055249264·PrimePadPlus-K2-3422
REUSABLE LAPAROSCOPIC CLIP APPLIER WITH IMPLANTABLE TITANIUM CLIPS
FDA Adverse Event
Malfunction
·MICROLINE SURGICAL, INC·Product code FZP·April 24, 2017
REUSABLE LAPAROSCOPIC CLIP APPLIER WITH IMPLANTABLE TITANIUM CLIPS
FDA Adverse Event
Malfunction
·MICROLINE SURGICAL, INC.·Product code FZP·April 24, 2017
REUSABLE LAPAROSCOPIC CLIP APPLIER WITH IMPLANTABLE TITANIUM CLIPS
FDA Adverse Event
Malfunction
·Product code FZP·April 24, 2017
REUSABLE LAPAROSCOPIC CLIP APPLIER WITH IMPLANTABLE TITANIUM CLIPS
FDA Adverse Event
Malfunction
·MICROLINE SURGICAL, INC.·Product code FZP·April 24, 2017
REUSABLE LAPAROSCOPIC CLIP APPLIER WITH IMPLANTABLE TITANIUM CLIPS
FDA Adverse Event
Malfunction
·Product code FZP·April 24, 2017
RENEW LAPCLINCH GRASPER TIP, REUSABLE
FDA Adverse Event
MICROLINE SURGICAL, INC.·Product code GEI·February 2, 2017
RENEW LAPCLINCH GRASPER TIP, REUSABLE
FDA Adverse Event
Malfunction
·MICROLINE SURGICAL, INC.·Product code GEI·February 2, 2017
DISPOSABLE 19 MEDIUM/LARGE TITANIUM K2 CLIP CART
FDA Adverse Event
Malfunction
·MICROLINE SURGICAL INC.·Product code GCJ·November 9, 2017
Dental sensors NanoPix1, NanoPix2
FDA 510(k)
FDA Class 2
·Dental
EkoSonic Endovascular Device, EKOS+ Endovascular Device
FDA 510(k)
FDA Class 2
·Cardiovascular
DISPOSABLE 19 MEDIUM/LARGE TITANIUM K2 CLIP CART
FDA Adverse Event
Malfunction
·MICROLINE SURGICAL INC.·Product code GCJ·November 9, 2017
DISPOSABLE 19 MEDIUM/LARGE TITANIUM K2 CLIP CART
FDA Adverse Event
Malfunction
·MICROLINE SURGICAL INC.·Product code GCJ·November 9, 2017
ML-10 MUTI-FIRE CLIP APPLIER
FDA Adverse Event
Malfunction
·MICROLINE SURGICAL INC.·Product code GCJ·November 9, 2017
RENEW ENDOCUT SCISSOR TIP, REUSABLE
FDA Adverse Event
Malfunction
·MICROLINE SURGICAL, INC.·Product code GEI·March 4, 2017
RENEW ENDOCUT SCISSOR TIP, REUSABLE
FDA Adverse Event
Malfunction
·MICROLINE SURGICAL, INC.·Product code GEI·March 5, 2017
1223422-2006-00001
FDA Adverse Event
Other
·Product code GEI·February 2, 2006