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