40 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NC SP02 ADAPTER CABLE
FDA 510(k)
FDA Class 2
·Cardiovascular
OsteoMed
FDA UDI
OSTEOMED LLC·00845694000475·1.2mm x 4mm Screw
SOAR Retractor System
FDA UDI
SPINEOLOGY INC.·M7403041204·12mm x 40mm Portal Tube
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0112040·Tap, 6.5 mm
OsteoMed
FDA UDI
OSTEOMED LLC·00845694028868·1.2mm x 4mm Screw, Sterile
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0112040·Tap, 5.50mm
OsteoMed
FDA UDI
OSTEOMED LLC·00845694054386·1.2mm x 4mm Screw Sterile Qty 10
ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822
FDA 510(k)
FDA Class 2
·Cardiovascular
NEUROFAX, MODELS EEG-1100A, EEG-9100A
FDA 510(k)
FDA Class 2
·Neurology
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026
ENDOTAK C
FDA Adverse Event
Injury
·HISTORICAL CPI ST. PAUL·Product code NVY·April 8, 2013
MALLINCKRODT
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code BTR·March 29, 2011
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS CORP.·Product code LFR·May 9, 2008
BD PHOENIX¿ SMIC/ID-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 16, 2024
BD PHOENIX¿ SMIC/ID-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 1, 2024
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 28, 2025
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 28, 2025
INCLUSIVE TAPERED IMPLANT 3.7MMD X 10MML X 3.5MMP
FDA Adverse Event
Malfunction
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·April 3, 2020
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 28, 2025
BD PHOENIX¿ SMIC/ID-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 8, 2024