11 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Tigertriever 13 Revascularization Device
FDA 510(k)
FDA Class 2
·Cardiovascular
Zavation
FDA UDI
Zavation LLC·00842166133006·Ti3Z CIF 14mmx16mmx8mm -8 deg
ZAVATION
FDA UDI
Zavation LLC·00842166105096·CIF 14x16, 8 deg, -08
FERTILITE OV
FDA 510(k)
FDA Class 1
·Clinical Chemistry
EXPORT XT CATHETER, EXPORT AP CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
ENDO MODEL M
FDA Adverse Event
Malfunction
·WALDEMAR LINK GMBH & CO. KG·Product code HRY·February 13, 2024
HEMOSTASIS VALVE INTRODUCERS
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES, PR·Product code DYB·October 30, 2008
BONE SCREW 76353200 REPOSE SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC·Product code LRK·August 23, 2011
UNKNOWN DEPUY FEMORAL PROTHESIS
FDA Adverse Event
Injury
·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 11, 2013
ENDO MODEL M
FDA Adverse Event
Malfunction
·WALDEMAR LINK GMBH & CO. KG·Product code HRY·February 13, 2024
Torcon NB Advantage Catheters - Product Usage: Intended for use in the peripheral and coronary vascular system, including the carotid arteries, in giographic procedures by physicians trained and experienced in angiographic techniques.
FDA Enforcement
Class II
·Terminated·Cook Inc.·November 27, 2019