9 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Health Line CT CVC
FDA 510(k)
FDA Class 2
·General Hospital
ROTATING GAMMA SYSTEM INFINI (INFINI)
FDA 510(k)
FDA Class 2
·Radiology
FORCE FIBER BLUE ULTRA HIGH MOLECULAR WEIGHT POLYETHYLENE NON ABSORBABLE SUTURES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BD VACUTAINER® ECLIPSE¿ BLOOD COLLECTION NEEDLE WITH PRE-ATTACHED HOLDER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code FMI·November 26, 2024
BD VACUTAINER® ECLIPSE¿ BLOOD COLLECTION NEEDLE WITH PRE-ATTACHED HOLDER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code FMI·December 9, 2024
FLEXCATH STEERABLE SHEATH
FDA Adverse Event
Injury
·MEDTRONIC CRYOCATH LP·Product code DRA·August 5, 2011
CORTSCR Ø1.5 L16 SST
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HWC·June 27, 2013
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·October 22, 2014
TrueBeam Radiotherapy Delivery System version 2.0 and 2.5 EDGE Radiotherapy Delivery System version 2.0 and 2.5 Product Usage: The TrueBeam delivery systems are intended to provide radiotherapy and stereotactic radiosurgery for lesions, tumors, and conditions anywhere in the body where radiation treatment is indicated.
FDA Enforcement
Class II
·Terminated·Varian Medical Systems·October 10, 2018