14 results
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20ms
·
Sources: EU EUDAMED, US FDA
BE PLUS / AURA-LTM64 AMPLIFIER
FDA 510(k)
FDA Class 2
·Neurology
SOLIDEA
FDA UDI
CALZIFICIO PINELLI SRL·08300496053606·MICROMASSAGE ARMBANDS CCL1, SIZE S, FUCSIA, GRA...
JOBST forMen
FDA UDI
BSN MEDICAL, INC.·04042809843910·FOR MEN 30-40 MM HG KNEE HIGH CLOSED TOE SMALL-...
TILITE YG AND TILITE YGS
FDA 510(k)
FDA Class 1
·Physical Medicine
ACS 180 HOMOCYSTEINE ASSAY
FDA 510(k)
FDA Class 2
·Clinical Chemistry
THINLINE II
FDA Adverse Event
Injury
·GUIDANT ANGLETON/ST. PAUL·Product code NVN·April 11, 2013
ACUITY
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·April 13, 2011
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code NIQ·May 23, 2008
12/14 ARTICUL 40MM M SPEC+5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·April 9, 2013
PINNACLE MTL INS NEUT40IDX56OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·April 9, 2013
11/13 S-ROM 40MM M SPEC+6
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·November 17, 2012
PINNACLE MTL INS NEUT40IDX56OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 17, 2012
Sigma implantable pulse generators (IPGs) Dual Chamber Atrial Sensing, Ventricular Sensing and Pacing Pacemaker. Atrial Bipolar sensing connector, ventricular Bipolar connector, model SVDD303.
FDA Recall
Terminated
·Medtronic Inc. Cardiac Rhythm Managment·Product code DXY·November 29, 2005
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