10 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Full Automatic (NIBP) Blood Pressure Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
NA
FDA UDI
MAKO SURGICAL CORP.·00848486003166·HIP PROBE
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613084837·K-Wire, Double Ended, Trocar Point, Diameter 0....
World Smart Card Size 8
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215046354·
MULTICODE - RTX HERPES SIMPLEX VIRUS 1 AND 2 KIT, MODEL 3711
FDA 510(k)
FDA Class 2
·Microbiology
NAVITRACK SYSTEM-OS KNEE UNIVERSAL, MODEL PRO-05002
FDA 510(k)
FDA Class 2
·Neurology
ARGYLE DUAL LUMEN UMBILICAL VESSEL CATHETER
FDA Adverse Event
Malfunction
·SHERWOOD DAVIS AND GECK·Product code FOS·November 22, 1996
SYBRONPRO TL
FDA Adverse Event
Injury
·EBI INC.·Product code DZE·July 13, 2011
SPRINT FIDELIS
FDA Adverse Event
Injury
·MPRI·Product code LWS·June 10, 2013
COLLEAGUE CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 16, 2008