17 results
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35ms
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Sources: EU EUDAMED, US FDA
ELECTROENCEPHALOGRAPHS EEG-5208,5210
FDA 510(k)
FDA Class 2
·Neurology
Ultraverse® 018
FDA UDI
Bard Peripheral Vascular, Inc.·00801741156557·Ultraverse® 018 PTA Balloon Dilatation Catheter...
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209128549·
POWDER FREE NITRILE PATIENT EXAMINATION GLOVE, BLUE, WHITE AND GREEN COLORED. NON-STERILE, LOW DERMATITIS POTENTIAL
FDA 510(k)
FDA Class 1
·General Hospital
Medical Nitrile Examination Gloves
FDA 510(k)
FDA Class 1
·General Hospital
NA
FDA UDI
STRYKER CORPORATION·04546540362377·1.6mm Cross-Cut Fissure Extended
NA
FDA UDI
STRYKER CORPORATION·04546540362346·1.2mm Cross-Cut Fissure
NA
FDA UDI
STRYKER CORPORATION·04546540362360·2.1mm Cross-Cut Fissure
NA
FDA UDI
STRYKER CORPORATION·04546540467638·3.2mm Cross-Cut Fissure Extended
NA
FDA UDI
STRYKER CORPORATION·04546540362353·1.6mm Cross-Cut Fissure
NA
FDA UDI
STRYKER CORPORATION·04546540362384·2.1mm Cross-Cut Fissure Extended
NA
FDA UDI
STRYKER CORPORATION·04546540362339·1.0mm Cross-Cut Fissure
*
FDA Adverse Event
Malfunction
·COVIDIEN·Product code LWH·April 24, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 5, 2012
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 23, 2010
1.2mm Cross Cut Fissure - Intended for use in the cutting, drilling, reaming, decorticating, shaping and smoothing of bone, bone cement and teeth in a variety of surgical procedures including but not limited to dental, ENT (ear, nose and throat), neuro, spine and endoscopic applications Catalog Number: 5820-066-012
FDA Enforcement
Class II
·Ongoing·Stryker Corporation·October 23, 2024
1.2mm Cross Cut Fissure - Intended for use in the cutting, drilling, reaming, decorticating, shaping and smoothing of bone, bone cement and teeth in a variety of surgical procedures including but not limited to dental, ENT (ear, nose and throat), neuro, spine and endoscopic applications Catalog Number: 5820-066-012
FDA Recall
Open, Classified
·Stryker Corporation·Product code HBE·September 5, 2024