9 results
·
17ms
·
Sources: EU EUDAMED, US FDA
RSI FEMORAL GUIDING CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
ASPIRATING SYRINGE, NON-ASPIRATING SYRINGE
FDA 510(k)
FDA Class 2
·Dental
WHEELCHAIR, MECHANICAL SERIES MODEL 3100
FDA 510(k)
FDA Class 1
·Physical Medicine
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE REHABILITATION EQUIP·Product code FSA·June 30, 2014
KENDALL MONOJECT MAGELLAN 3ML SYRINGE WITH SAFETY
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FMF·November 12, 2010
TOTALCARE BARIATRIC PLUS BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·November 29, 2012
WITTICH NITINOL STONE BASKET
FDA Adverse Event
Malfunction
·COOK INC·Product code LQR·February 20, 2019
WITTICH NITINOL STONE BASKET
FDA Adverse Event
Malfunction
·COOK INC·Product code LQR·February 20, 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