12 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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LDR SPINE EASYSPINE POSTERIOR OSTEOSYNTHESIS SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
FLI
FDA UDI
Rmo, Inc.·00885797550538·FLI CUNITI PREFORMED EXPANDED ARCH MX/MN .014 X...
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306814389·Mixter Hemostatic Forceps, Strongly Curved, 16 cm
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306814983·Mixter Hemostatic Forceps, Strongly Curved, 16 cm
GIVEN DIAGNOSTIC SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MEDTRONIC PS MEDICAL MURPHYSCOPE, MODELS 2125-032, 2125033,2125-042, 2125-043, 2125-157, 2125-158,2125-161 2125-162,,
FDA 510(k)
FDA Class 2
·Neurology
SPECTRA WAVEWRITER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 3, 2024
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·December 17, 2018
TIBIAL ARTICULAR SURFACE PROVISIONAL
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JWH·December 20, 2018
SAGITTAL SAW ATTACHMENT FOR TRAUMA RECON SYSTEM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HWE·April 22, 2013
6083 AMBULANCE COT
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·April 18, 2011
GE OEC 8800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 9, 2008