20 results
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54ms
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Sources: EU EUDAMED, US FDA
RadiForce Large Monitor System
FDA registration
EIZO GmbH·1 product·🇩🇪 Germany
RADIFORCE LARGE MONITOR SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
Display, Cathode-Ray Tube, Medical
FDA classification
FDA Class 2
·Display, Cathode-Ray Tube, Medical
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741126450·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674112645060·
PIVOX™ Oblique Lateral Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169605343·SPACER 2112645 OLIF25 20MM 12 DEG 18X45
2810 3WAY SLIDE VALVE
FDA UDI
HANS RUDOLPH, INC.·00874750009336·2810C 3W SLDVL 1.375OD/1.125ID
Reprocessed External Fixation Device
FDA registration
Stryker Sustainability Solutions·3 products·🇺🇸 United States
Creagh8289 (TL) - First Choice
FDA registration
Synergy Health Ireland Ltd·2 products·🇮🇪 Ireland
component, traction, invasive Reprocessed External Fixation Devices
FDA registration
Sterigenics US LLC·3 products·🇺🇸 United States
FirstChoice Ultra High Pressure PTA Balloon Catheters
FDA registration
Creagh Medical Ltd.·2 products·🇮🇪 Ireland
Reprocessed External Fixation Device
FDA registration
Stryker Sustainability Solutions Phoenix·3 products·🇺🇸 United States
Velocity™ Expandable Interbody System
FDA UDI
Spine Wave, Inc.·10840642106916·Expandable Implant, 25(L) X 10(W) X 8-14(H) 8 D...
Algovita®
FDA UDI
Greatbatch Ltd·00821329580222·Algovita® 12 Electrode Percutaneous Lead Kit - ...
XN-10
FDA registration
SYSMEX CORPORATION i-SQUARE·1 product·🇯🇵 Japan
RegenerOss Putty Plus
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States
WILLOW/ELM PTA BALLOON DILATATION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
REPROCESSED EBI EXTERNAL FIXATION DEVICES
FDA 510(k)
FDA Class 2
·Orthopedic
Appliance, Fixation, Nail/Blade/Plate Combination, Single Component
FDA classification
FDA Class 2
·Appliance, Fixation, Nail/Blade/Plate Combination, Single Component
Catheter, Angioplasty, Peripheral, Transluminal
FDA classification
FDA Class 2
·Catheter, Angioplasty, Peripheral, Transluminal