9 results
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21ms
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Sources: EU EUDAMED, US FDA
SMARTSUCTION SOLO DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MPS M ELECTRODE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
N2000 BASE STATION, N2001 NURSE STATION
FDA 510(k)
FDA Class 2
·Cardiovascular
UNKNOWN FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·April 16, 2019
HELICAL BLADE COUPLING SCREW
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code LXH·April 17, 2013
LIGASURE PRECISE
FDA Adverse Event
Malfunction
·COVIDIEN LP (VALLEYLAB)·Product code GEI·June 17, 2008
CURLIN ADMINISTRATON SET
FDA Adverse Event
Other
·MOOG MEDICAL DEVICES GROUP·Product code FRN·April 7, 2011
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
CADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120, Version 1.0. Provide measured drug therapy to patients in hospital or outpatient settings.
FDA Enforcement
Class II
·Terminated·Smiths Medical ASD, Inc.·June 24, 2015