8 results
·
25ms
·
Sources: EU EUDAMED, US FDA
CARDIMAX FX-406U
FDA 510(k)
FDA Class 2
·Cardiovascular
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209130306·
HUMAN SERUM ELECTROLYTE CONTROL-LIQUID
FDA 510(k)
FDA Class 1
·Clinical Chemistry
DESERET EPIDURAL CATHETER W/TOUGHY-BORST ADAPTER
FDA 510(k)
FDA Class 2
·Anesthesiology
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 6, 2014
PUMP IN STYLE ADVANCED BREAST PUMP GO TOTE
FDA Adverse Event
Malfunction
·MEDELA, INC.·Product code HGX·November 29, 2012
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MKJ·September 30, 2010
Alcon Custom Pak
FDA Enforcement
Class II
·Ongoing·Alcon Research, LTD.·August 23, 2023