10 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ZIMMER M/L TAPER HIP PROSTHESIS WITH KINECTIV TECHNOLOGY SYSTEM, MODEL(S) 7848 SERIES( MODULAR NECKS), 7713 SERIES
FDA 510(k)
FDA Class 3
·Orthopedic
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704294231·
RADIOGRAPHIC MARKERS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SUPERCROSS CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
MECHANICAL WALKER, ROLLATOR
FDA Adverse Event
DANYANG MAXTHAI MEDICAL EQUIPMENT·Product code ITJ·April 22, 2013
SYNVISC
FDA Adverse Event
Injury
·Product code MOZ·April 22, 2011
LIFEPAK 20 DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code LDD·July 8, 2008
BD ULTRA FINE¿ PEN NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·March 11, 2020
BD ULTRA-FINE¿ MINI PEN NEEDLES 5MM (3/16¿) 31G
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·October 9, 2019
Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone
FDA Enforcement
Class II
·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012