10 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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iCOquit® Smokerlyzer®
FDA 510(k)
FDA Class 2
·Anesthesiology
BD Microprobe™ Processor
FDA UDI
BECTON, DICKINSON AND COMPANY·00382902119180·BD Microprobe™ Processor
Curved Plate
FDA UDI
I.T.S. GmbH·09120034309632·Curved Plate, 8-Hole, PRS RX System
NIHON KOHDEN BSM-2300A SERIES BEDSIDE MONITOR AND ACCESSORIES, MODEL BSM-2300A SERIES
FDA 510(k)
FDA Class 2
·Cardiovascular
EVOS Large Fragment Plating System
FDA 510(k)
FDA Class 2
·Orthopedic
ASCENSIA CONTOUR TS
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE, LLC·Product code NBW·October 20, 2008
ENDOPATH** XCEL* TROCAR
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·August 15, 2011
MECHANICAL CHAIR/TRANSPORT CHAIR
FDA Adverse Event
DANYANG MAXTHAI MEDICAL EQUIPMENT·Product code INM·July 8, 2013
Model Number L211 PROPONENT DR SL MRI Pacemaker
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025
PROPONENT DR Pacemaker, SL (Model Number L201), (VDD) SL (Model Number L209), SL MRI (Model Number L211), EL (Model Number L221), and EL MRI (Model Number L231).
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·January 22, 2025