17 results
·
41ms
·
Sources: EU EUDAMED, US FDA
VITEK 2 AST- Gram Negative Polymyxin B
FDA registration
BIOMERIEUX, INC.·3 products·🇺🇸 United States
VITEK 2 AST- Gram Negative Polymyxin B
FDA registration
bioMerieux, Inc.·3 products·🇺🇸 United States
VITEK 2 AST- Gram Negative Polymyxin B (<=0.25 >=16 ug/mL)
FDA 510(k)
FDA Class 2
·Microbiology
EarQ
FDA UDI
Oticon A/S·05707131343482·G10, MINIRITE T 312 2.4G C090 EARQ
MatrixMANDIBLE Reconstruction Plates
FDA registration
Synthes (USA) Products LLC·1 product·🇺🇸 United States
Physio Control LifePak 15 Defibrillator
FDA registration
EMS SURPLUS CANADA·1 product·🇨🇦 Canada
SYNTHES MATRIXMADIBLE PLATE AND SCREW SYSTEM
FDA registration
EXEL INC. DBA DHL SUPPLY CHAIN (USA)·1 product·🇺🇸 United States
CABLE-EXTERNAL POWER, RIGHT ANGLE
FDA registration
BERND RICHTER GMBH·1 product·🇩🇪 Germany
PLATE, BONE
FDA registration
SYNTHES GMBH·1 product·🇨🇭 Switzerland
Jabil Inc. (Elmira)
FDA registration
Jabil Inc. (Elmira)·1 product·🇺🇸 United States
ZELTIQ AESTHETICS, INC.
FDA registration
ZELTIQ AESTHETICS, INC.·1 product·🇺🇸 United States
HARH23,HARH36,HARH45
FDA registration
MDTGLOBAL, A.S.·2 products·🇸🇰 Slovakia
System, Test, Automated, Antimicrobial Susceptibility, Short Incubation
FDA classification
FDA Class 2
·System, Test, Automated, Antimicrobial Susceptibility, Short Incubation
ACTIVE KNEE TOTAL KNEE REPLACEMENT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
LIFEPAK 15 MONITOR/DEFIBRILLATOR
FDA 510(k)
FDA Class 3
·Cardiovascular
Automated External Defibrillators (Non-Wearable)
FDA classification
FDA Class 3
·Automated External Defibrillators (Non-Wearable)
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
FDA classification
FDA Class 2
·Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer