12 results
·
18ms
·
Sources: EU EUDAMED, US FDA
LV-20 VOLUMETER, 20 MHZ DOPPLER BLOOD FLOW METER
FDA 510(k)
FDA Class 2
·Cardiovascular
Brigade
FDA UDI
Nuvasive, Inc.·00887517190536·Brigade Trial, 20x34x24mm 8°
LEONE SPA
FDA UDI
LEONE SPA·08033707059929·DB BRACKET 34 EXTREMO NO-Ni 22 T-17
75H - Class A MRO 21 - w/Select Logo
FDA UDI
Certified Safety Manufacturing, Inc.·00766588620343·75H - Class A MRO 21 - w/Select Logo
Color Cuff
FDA UDI
STRYKER CORPORATION·07613154600106·Non-Sterile Reusable Tourniquet Cuff Single Bla...
Color Cuff
FDA UDI
STRYKER CORPORATION·07613154600090·Non-Sterile Reusable Tourniquet Cuff Single Bla...
Color Cuff
FDA UDI
STRYKER CORPORATION·07613154600113·Non-Sterile Reusable Tourniquet Cuff Single Bla...
MRJ 3300
FDA 510(k)
FDA Class 2
·Radiology
RightLance Blood Lancing System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
AVAULTA SOLO SYNTHETIC SUPPORT SYSTEM - ANTERIOR
FDA Adverse Event
Injury
·C.R. BARD, INC. (COVINGTON)·Product code FTL·January 4, 2013
HEARTSTART MRX-EMS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MKJ·December 8, 2010
FINELINE II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code DTB·July 9, 2014