11 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KARL STORZ BOUGIES, SOUNDS, DILATORS
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704268997·
3.0 FR GROSHONG PERIPHER INSERT CENT VENOUS CATH
FDA 510(k)
FDA Class 2
·General Hospital
KERATIN PRIMARY ANTIBODY
FDA 510(k)
FDA Class 2
·Immunology
ACCU-CHEK ® COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·February 6, 2013
AUTOMATED PD SET W/CASSETTE4 PRONG
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 4, 2011
1 DAY TRUEYE (NARAFILICON A) CONTACT LENS
FDA Adverse Event
Injury
·VISTAKON·Product code LPL·July 10, 2014
VASOVIEW HEMOPRO 2
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR LLC·Product code GEI·January 5, 2024
VASOVIEW HEMOPRO 2
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR LLC·Product code GEI·January 5, 2024
VASOVIEW HEMOPRO 2
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR LLC·Product code GEI·January 5, 2024
VASOVIEW HEMOPRO 2
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR LLC·Product code GEI·January 5, 2024