7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
SINGLE & DUAL CHANNEL RECORDER
FDA 510(k)
FDA Class 1
·Cardiovascular
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR27720481·DuoForce wires max. .019"x.025"
LUMACARE MODEL LC-122M NON-COHERENT LIGHT SOURCE AND MODEL LUM-P FIBRE OPTIC PROBE
FDA 510(k)
FDA Class 2
·Physical Medicine
FluidSmart
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
IV3000 1 HAND 6X7CM
FDA Adverse Event
SMITH AND NEPHEW MEDICAL LIMITED·Product code KGX·April 25, 2014
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·November 2, 2007
NXSTAGE SYSTEM ONE
FDA Adverse Event
Injury
·NXSTAGE MEDICAL, INC.·Product code KDI·September 28, 2012