8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACCUSIGN BAR-RAPID ONE-STEP BARBITURATE ASSAY
FDA 510(k)
FDA Class 2
·Clinical Toxicology
SURGISTAR
FDA UDI
SURGISTAR, INC.·00878799000835·
ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
BPA, BODY POSITION ALARM
FDA 510(k)
FDA Unclassified
·Unknown
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·September 25, 2025
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·June 18, 2014
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 14, 2013
OCTRODE PERCUTANEOUS LEADS
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·January 13, 2011