8 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ELECTRIC HANDPIECE SYSTEM
FDA 510(k)
FDA Class 1
·Dental
RC Screw-retained Abutment
FDA UDI
BIO CONCEPT Co., Ltd.·06947600381211·
Bernafon
FDA UDI
Bernafon AG·05711584051016·CA3 ITCPD, WL R BE CARISTA 3
POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (YELLOW)
FDA 510(k)
FDA Class 1
·General Hospital
CENTRICITY CARDIO IMAGING
FDA 510(k)
FDA Class 2
·Radiology
LOCKSCR Ø3.5 SELF-TAP L10 TAN
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code KTT·May 29, 2013
C-QUR V PATCH
FDA Adverse Event
Injury
·ATRIUM MEDICAL CORP.·Product code FTL·September 24, 2014
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·June 17, 2011