25 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Polysafety BC, Polysafety BC Adva, Polywin Safety, Polywin Safety Adva
FDA 510(k)
FDA Class 2
·General Hospital
BD BBL™ Gram Slide
FDA UDI
BECTON, DICKINSON AND COMPANY·30382902314012·BD BBL™ Gram Slide, 50
OMNI Mod Hip
FDA UDI
Omni Life Science, Inc.·00841690130147·Modular Neck 13 degree Anteversion, Medium 35
Intrigue
FDA UDI
LANCER ORTHODONTICS, INC.·00817573021758·OPTYC MBT CEN +17T +4A 018 UR
YLB-IOFA- Large
FDA UDI
NEOCIS INC·00810004900578·YLB-IOFA- Large
FIXION DYNAMIC HIP SCREW SYSTEM (FIXION DHS)
FDA 510(k)
FDA Class 2
·Orthopedic
BLOWFISH TRANSBRONCHIAL MICRO-INFUSION CATHETER
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
ADVANCED NEURON DELIVERY CATHETER 070
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DQY·October 2, 2009
PYRENEES® Cervical Plate System
FDA UDI
VB Spine LLC·10888857241978·Translational Plate, Compressor
NEURON DELIVERY CATHETER 070
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DQY·March 29, 2010
NEURON DELIVERY CATHETER 070 ADVANCED
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DQY·October 27, 2009
NEURON DELIVERY CATHETER 070
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DQY·March 16, 2010
NEURON DELIVERY CATHETER 070 ADVANCED
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DQY·November 13, 2009
NEURON DELIVERY CATHETER 070 ADVANCED
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DQY·November 13, 2009
RESERVOIR 3ML
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code FRN·July 18, 2011
TENDRIL STS
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·November 6, 2014
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 12, 2013
NEURON DELIVERY CATHETER 070
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DQY·March 4, 2010
ADV. NEURON DELIVERY CATHETER 070
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DQY·March 16, 2010
NEURON DELIVERY CATHETER 070
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DQY·March 16, 2010