9 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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V-Laser
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SYRINGE 50ML LL TIP 1ML
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMF·November 4, 2024
BD LUER-LOK
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY·Product code FMF·November 26, 2024
NON STERILE POWDER FREE NITRILE EXAMINATION GLOVES, BLUE
FDA 510(k)
FDA Class 1
·General Hospital
V.A.C. VERAFLO CLEANSE DRESSING SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
AUTOLUBE-III
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code GEY·October 17, 2014
K-WIRE Ø2 THREAD-TIP L280 SST
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HWC·June 21, 2013
VOYAGER OTW CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·July 28, 2011
BELIFU
FDA Adverse Event
Injury
·HONG QIANGXING (SHEN ZHEN) ELECTRONICS LIMITED·Product code GZJ·February 10, 2020