29 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MOTEX NITRILE EXAMINATION GLOVES POWDER-FREE
FDA 510(k)
FDA Class 1
·General Hospital
Aligned Medical Solutions
FDA UDI
Aligned Medical Solutions·B09800132610·Minor Procedure Pack
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450125892·
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0132110·Trial, TLIF, 27L OB CRV 7Deg, 11mm
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033468500·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033468548·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033468524·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033468579·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033468531·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033468562·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033468555·
CREATININE PLUS
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CARDIOMEDICS ECP SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
PROMUS ELEMENT PLUS EVEROLIMUS-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·March 20, 2013
CRYOVALVE PULMONARY VALVE & CONDUIT
FDA Adverse Event
Injury
·CRYOLIFE, INC.·Product code MIE·March 10, 2011
FLUENCY PLUS TRACHEOBRONCHIAL STENT GRAFT
FDA Adverse Event
Malfunction
·ANGIOMED GMBH & CO. MEDIZINTE·Product code JCT·March 14, 2008
BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·July 31, 2019
Q-SYTE CLOSED LUER ACCESS DEVICE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·November 13, 2020
BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·July 8, 2022
BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·March 7, 2018