11 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BIP-COAX-SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HIGH VOLTAGE PULSED GALVANIC STIMULATION APPLICATI
FDA 510(k)
FDA Class 2
·Physical Medicine
CEMAX SPARCSTATION IMAGING SOFTWARE AND WORKSTATIO
FDA 510(k)
FDA Class 2
·Radiology
GLIDEWIRE GT
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 30, 2026
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 12, 2014
DYONICS
FDA Adverse Event
Malfunction
·SMITH AND NEPHEW·Product code HRX·November 12, 2010
AUTOSONIX ULTRA SHEARS LONG
FDA Adverse Event
Malfunction
·COVIDIEN LP, FORMERLY US SURGICAL·Product code LFL·December 6, 2012
GLIDEWIRE GT
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 29, 2026
RADIFOCUS GLIDEWIRE
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 26, 2025
TERUMO RADIFOCUS GUIDE WIRE
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 3, 2025
GLIDEWIRE GT
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 21, 2018