11 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MEGA(TM) 7.5FR. 30CC INTRA-AORTIC BALLOON CATHETER AND ACCESSORIES, MEGA(TM) 7.5FR. 40CC INTRA-AORTIC BALLOON CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
MEGA 7.5FR. 40CC
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - FAIRFIELD·Product code DSP·February 10, 2020
Unity Total Knee System
FDA UDI
CORIN LTD·05056139243585·UNITY KNEE™ PS-C INSERT - Size 8T-7F x 18mm
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319704110·Bishop-Harmon Tissue Forceps 3-3/8" (8.6cm), st...
CASHMERE NON-STERILE, POWDER FREE NITRILE EXAMINATION GLOVES (WHITE)
FDA 510(k)
FDA Class 1
·General Hospital
CONFORMIS ITOTAL CR KNEE REPLACEMENT SYSTEM (KRS)
FDA 510(k)
FDA Class 2
·Orthopedic
FOGARTY OCCLUSION CATHETER
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES, PR·Product code MJN·May 20, 2013
SELOX ST 60
FDA Adverse Event
Injury
·BIOTRONIK GMBH AND CO.·Product code DTB·August 15, 2008
MINICAP TRANSFER SET
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·June 11, 2011
FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN, COLLAGEN SCAFFOLD WITH MET
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·August 11, 2020
VERSE POLY DRIVER SHAFT NAV
FDA Adverse Event
Malfunction
·DEPUY SPINE INC·Product code OLO·April 29, 2022