9 results
·
20ms
·
Sources: EU EUDAMED, US FDA
MODIFICATION TO RADIUS SNARE
FDA 510(k)
FDA Class 2
·Cardiovascular
EXPRO ELITE SNARE
FDA Adverse Event
Injury
·VASCULAR SOLUTIONS, INC·Product code MMX·June 19, 2017
SOLIDEA
FDA UDI
CALZIFICIO PINELLI SRL·08300496071457·STRIPE GAME COSMO, SIZE XL, NERO, GRADUATED COM...
ALOKA SSD-5500 WITH KI AND A-SMA
FDA 510(k)
FDA Class 2
·Radiology
FLEX SPAN TEMPORARY CROWN & BRIDGE MATERIAL
FDA 510(k)
FDA Class 2
·Dental
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·April 22, 2013
XMAX MOTOR
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code ERL·September 9, 2014
UNKNOWN DEPUY ASR FEMORAL HEAD
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KXA·April 13, 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