14 results
·
19ms
·
Sources: EU EUDAMED, US FDA
MASEP SRRS GAMMA RAYS STEREOTACTIC RADIATION THERAPY SYSTEM FOR HEADS (MASEP GAMMA THERAPY SYSTEM)
FDA 510(k)
FDA Class 2
·Radiology
Flex
FDA UDI
Diversified Products, Inc.·00037741504115·
Arthrex®
FDA UDI
ARTHREX, INC.·00888867522497·Cannulated Canc Screw,36mm Thd,7.0x125mm
AOS CANNULATED CANCELLOUS SCREW, 36mm THREAD 7.0mm x 125mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665010114·
Flex
FDA UDI
Diversified Products, Inc.·00842894114742·
NASAL CANNULA, WITH AND WITHOUT SUPPLY TUBING, AND OTHER SIMILAR NASAL CANNULA MANUFACTURED BY HRCI
FDA 510(k)
FDA Class 1
·Anesthesiology
GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING
FDA 510(k)
FDA Class 1
·Ophthalmic
FENESTRATED BIPOLAR FORCEPSINSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·December 4, 2013
INSIGNIA
FDA Adverse Event
Malfunction
·GUIDANT CLONMEL IRELAND·Product code NVZ·April 8, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 23, 2011
XIA LP POLYAXIAL SCREW 5.5 X 45MM
FDA Adverse Event
Injury
·STRYKER SPINE BORDEUX·Product code HWC·May 6, 2008
BD VACUTAINER® SODIUM FLUORIDE/POTASSIUM OXALATE 100 MG/20 MG
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·December 28, 2018
BD VACUTAINER® BLOOD ALCOHOL DETERMINATIONS SODIUM FLUORIDE: POTASSIUM OXALATE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·June 25, 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