8 results
·
26ms
·
Sources: EU EUDAMED, US FDA
CONNECT. DIAG. TOTAL PROTEIN DIAG. REAGE
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Epimed
FDA UDI
EPIMED INTERNATIONAL, INC·00818788021380·Wiley Spinal™
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668111086·INSTRUMENT CASE LARGE ALUMINUM
OptoMonitor
FDA 510(k)
FDA Class 2
·Cardiovascular
CATHETERIZATION KIT 732016-732018
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
INSTATRAK 3500
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code LLZ·January 10, 2014
OPEN-END URETERAL CATHETER
FDA Adverse Event
Injury
·COOK UROLOGICAL, INC.·Product code GBL·October 12, 2012
PERCUTANEOUS INSERTION HANDLE
FDA Adverse Event
Injury
·SYNTHES HAGENDORF·Product code LXH·May 22, 2015