10 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
CRYOMATIC MKII CONSOLE, CRYOMATIC MKII PROBES, DISPOSABLE CRYO PROBES
FDA 510(k)
FDA Class 2
·Ophthalmic
Oticon
FDA UDI
Oticon A/S·05707131256201·NERA PRO, BTE 13 WL 100 DBL
DUOLINK II
FDA 510(k)
FDA Class 2
·Dental
SMITH & NEPHEW IUR MORCELLATION SYSTEM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
CLEARVIEW UTERINE MANIPULATOR
FDA Adverse Event
Injury
·CLINICAL INNOVATIONS, LLC·Product code LKF·June 11, 2024
EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE
FDA Adverse Event
Malfunction
·AIZU OLYMPUS CO., LTD.·Product code FDS·July 22, 2022
TELIGEN
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 1, 2014
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 29, 2013
ENRHYTHM DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code DXY·June 16, 2011
FUSION 8MM-40CM UNSUPP PERIPHERAL GRAFT
FDA Adverse Event
Malfunction
·MAQUET CV·Product code DSY·February 8, 2017