7 results
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17ms
·
Sources: EU EUDAMED, US FDA
ACUPRESS VIBRATOR
FDA 510(k)
FDA Class 1
·Physical Medicine
ERA® Implant Abutment Micro Ang. Base, 3mm Cuff (K)
FDA UDI
STERNGOLD DENTAL LLC·00841549105722·Implant retained overdentures are an establishe...
ENFLOW IV FLUID WARMER
FDA 510(k)
FDA Class 2
·General Hospital
POLY PER-Q-CATH SINGLE LUMEN PICC CATHETER, MODEL 3143100; POLY PER-Q-CATH DUAL LUMEN PICC CATHETER, MODEL 3246100
FDA 510(k)
FDA Class 2
·General Hospital
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·May 15, 2014
PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA, INC.·Product code LWP·October 31, 2012
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·August 16, 2010