11 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KERLIX MD ANTIMICROBIAL GAUZE DRESSING
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
MEGA PLUS MIS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809665589705·MIS Fenestrated Screw M, Ø10.5 x 30mm, Ø6.0mm Rod
SPIN-LOC SUTURE ANCHOR SYSTEM FG-0302-01,FG-0305-01
FDA 510(k)
FDA Class 2
·Orthopedic
PUSH BALL INCLINE
FDA 510(k)
FDA Class 1
·Physical Medicine
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECES
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 8, 2006
NC QUANTUM APEX¿
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·March 5, 2013
EXCELLENCE+
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011
CARELINK
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code KRG·August 8, 2014
UNKNOWN
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·June 9, 2021
ZIMMON PANCREATIC STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·October 16, 2020
EMBRYO RPLCMNT CATHETER
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code MQF·September 24, 2019