313 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SYMBIA 6.0
FDA 510(k)
FDA Class 2
·Radiology
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756614528·Knee Immobilizer
LEONE SPA
FDA UDI
LEONE SPA·08033707010906·CALIBRA 1ST MOL BANDS W/G8025-02 n.UR 6
OsteoMed
FDA UDI
OSTEOMED LLC·00845694026468·MFx Angulated Locking Straight Plate, 4 Hole
CRYOMEGA
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
VITROS CHEMISTRY PRODUCTS DHDL SLIDES, VITROS CHEMISTRY PRODUCTS CALIBRATOR KIT 25, VITROS CHEMISTRY PRODUCTS PERFORMACE
FDA 510(k)
FDA Class 1
·Clinical Chemistry
I-STAT G3+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JJE·August 26, 2010
PEN NDL 32G 4MM 100BX 1200 USA
FDA Adverse Event
Malfunction
·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·February 10, 2025
STELLARTECH COAGULATION CATHETER
FDA Adverse Event
Injury
·STELLARTECH RESEARCH CORP·Product code KNQ·November 3, 2005
CONTOUR CURVED CUTTER STAPLER CS
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GDW·July 14, 2006
LIGAMAX 5
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC (CINCINNATI)·Product code FZP·April 17, 2007
HIRES 90K
FDA Adverse Event
Malfunction
·ADVANCED BIONICS CORP.·Product code MCM·September 5, 2006
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·December 12, 2006
NEXUS MULTI-DIAMETER CSR AND NXT HELIX SOFT
FDA Adverse Event
Injury
·EV3 NEUROVASCULAR·Product code HCG·December 18, 2008
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·June 23, 2006
HIRES 90K
FDA Adverse Event
Malfunction
·ADVANCED BIONICS CORPORATION·Product code MCM·May 9, 2006
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·August 9, 2006
INTERGARD AORTIC ARCH WOVEN VASCULAR PROSTHESIS
FDA Adverse Event
Injury
·INTERVASCULAR·Product code DSY·March 24, 2006
RENU
FDA Adverse Event
Injury
·BAUSCH AND LOMB·Product code LPN·May 17, 2006
ULTRACISION SURG DEV, CURVED SHEARS, ENDO
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GEI·July 14, 2006