8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DRLOCK DISTAL RADIUS VOLAR SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
TRIPLE LUMEN CENTRAL VENOUS CATHETER
FDA 510(k)
FDA Class 2
·General Hospital
ORTHOGENESIS LPS SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SCORPIOFLEX TOTAL KNEE PS
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·September 14, 2018
ANCHOR L SCREWDRIVER MODULAR FLEXIBLE
FDA Adverse Event
Malfunction
·STRYKER SPINE-FRANCE·Product code LXH·April 11, 2013
ACCU-CHEK AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·May 27, 2008
SPRINT QUATTRO SECURE
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·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