12 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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I-STAT CG8+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code CHL·May 25, 2023
i-STAT CHEM8+ cartridge with the i-STAT 1 System
FDA 510(k)
FDA Class 2
·Clinical Chemistry
I-STAT CHEM8+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JPI·December 17, 2024
Vanguard® Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304272132·
Vanguard Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304476721·
PULMONETIC SYSTEMS LTV 1200 MR CONDITIONAL VENTILATOR
FDA 510(k)
FDA Class 2
·Anesthesiology
G-PROX EZ ENDOSCOPIC GRASPER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
LTV 1200 VENTILATOR
FDA Adverse Event
Malfunction
·VYAIRE MEDICAL, INC·Product code CBK·November 13, 2023
UNICEL DXC 600 SYNCHRON CLINICAL SYSTEM
FDA Adverse Event
Injury
·BECKMAN COULTER, INC.·Product code JGS·July 22, 2011
M2A-MAGNUM MODULAR HEAD SIZE 44MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·June 22, 2013
COLLEAGUE CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 4, 2008
LTV 1200 VENTILATOR
FDA Adverse Event
Malfunction
·VYAIRE MEDICAL, INC·Product code CBK·December 13, 2023