11 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Puritan Bennett 980 Ventilator System
FDA 510(k)
FDA Class 2
·Anesthesiology
PURITAN BENNETT 980 SERIES VENTILATOR
FDA Adverse Event
Malfunction
·MEDTRONIC/COVIDIEN·Product code CBK·September 17, 2025
SMOOTH STEINMANN PINS, DOUBLE END TROCAR POINT
FDA UDI
Biomet Orthopedics, LLC·00887868016738·
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523139156·Broach, 38 X 30, 21mm Height 28° Hyperlordotic
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523139149·Broach, 38 X 30, 19mm Height 28° Hyperlordotic
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523139132·Broach, 38 X 30, 17mm Height 28° Hyperlordotic
ANDON HEALTH CARE MANAGEMENT SYSTEM SOFTWARE
FDA 510(k)
FDA Class 2
·Clinical Chemistry
LANX FUSION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
OT VERIO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 14, 2011
RADIAL JAW 3 SINGLE- USE BIOPSY FORCEPS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FCL·September 16, 2008