67 results · 28ms · Sources: EU EUDAMED, 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