Web17 dec. 2024 · The recall covers 11,299 SynchroMed II Models 8637-20 and 8637-40 manufactured between May 4, 2024, and April 5, 2024, including 7,317 pumps sold in … http://www.mrisafety.com/TMDL_list.php?mastertable=SafetyInformation&masterkey1=197
Compatibilité IRM des Dispositifs Médicaux
WebModellen 8637-20, 8637-40 Recall . Oktober 2024 . Medtronic Referentie: FA889 . Geachte zorgverlener, Deze brief is bedoeld om u te informeren dat Medtronic vrijwillig specifieke … WebThe recall includes the SynchroMed II Implantable Infusion Pump models 8637-20 and 8637-40, distributed between May 2004 and July 8, 2011. BACKGROUND: The SynchroMed II Implantable Programmable Drug Pump is part of the SynchroMed II Infusion system designed to contain and administer prescribed drugs to a specific site. burton ak jacket pink
PUMP 8637-20 SYNCHMED II 20ML EMAN SYMBL Medical Device …
WebMedtronic Manuals: Country and Language Manual Library Region > North America Please select the locale. Manuals may be available in additional languages, depending on the locale selected. Aruba Bahamas Barbados Belize Bermuda Canada Costa Rica Curaçao Dominican Republic El Salvador Greenland Guatemala Honduras Jamaica Mexico … Web1 mrt. 2016 · Medtronic heeft verbeteringen aangebracht aan de SynchroMed® II pomp, die de kans op kortsluiting van het interne elektrische circuit en motorcorrosie wat tot … WebPUMP 8637-20 SYNCHROMED II 20ML DLC US MEDTRONIC, INC. FDA.report GUDID MEDTRONIC, INC. 00643169984219 Implantable intrathecal infusion pump, programmableImplantable intrathecal infusion pump, programmable Customer Support Contacts Device Dimensions Operating and Storage Conditions Device Identifiers FDA … burton 159 jussi oksanen snowboard