List view Cards view
Name Classification Manufacturer Risk Class Country Source
Medtronic SynchroMed II Infusion Pump General Hospital and Personal Use Devices Medtronic Inc New Zealand NZMMDSA
SynchroMed EL Drug Infusion Pump General Hospital and Personal Use Devices Medtronic Inc New Zealand NZMMDSA
Medtronic Synchromed II Implantable Infusion Pump General Hospital and Personal Use Devices Medtronic Inc New Zealand NZMMDSA
SynchroMed® II pump General Hospital and Personal Use Devices Medtronic Inc New Zealand NZMMDSA
synchromed electronic implantable pumps General Hospital and Personal Use Devices MEDTRONIC Italy MSHM
Synchromed II General Hospital and Personal Use Devices MEDTRONIC France ANSM
Device Recall Synchromed II General Hospital and Personal Use Devices Medtronic Inc, Neurological & Spinal Division 2 United States USFDA
SynchroMed lmplantable Infusion Pump General Hospital and Personal Use Devices Medtronic Serbia ALIMSA
Synchromed II General Hospital and Personal Use Devices Medtronic Serbia ALIMSA
SynchroMed II Programmable Implantable Infusion Pump General Hospital and Personal Use Devices Medtronic Inc Serbia ALIMSA
SynchroMed II Programmable Implantable Infusion Pump General Hospital and Personal Use Devices Medtronic Inc. Serbia ALIMSA
SynchroMed II Programmable Implantable Infusion Pump General Hospital and Personal Use Devices Medtronic Inc. Serbia ALIMSA
infusion pump, SynchroMed EL implantable infusion pump General Hospital and Personal Use Devices Medtronic Neuromodulation Saudi Arabia SFDA
SynchroMed II Programmable Pump General Hospital and Personal Use Devices Medtronic Inc. Czechia MHSIDCCCDMIS
SynchroMed® II Progr. Pump, N'Vision Application C General Hospital and Personal Use Devices Medtronic Inc. Czechia MHSIDCCCDMIS
SynchroMed El Implantable General Hospital and Personal Use Devices Medtronic Inc Finland VNSAWH
Synchromed EL Implantable Pump General Hospital and Personal Use Devices Medtronic Inc. Switzerland SATP
Synchromed EL Implantable Pump, Model/Catalog 8626x-xx and 8627x-xx General Hospital and Personal Use Devices Medtronic Inc. Switzerland SATP
Synchromed EL Implantable Pump, General Hospital and Personal Use Devices Medtronic Inc. Switzerland SATP
SynchroMed II and SynchroMed EL Implantable Drug Pumps and Refill Kits General Hospital and Personal Use Devices Medtronic Inc. Switzerland SATP
SynchroMed II and SynchroMed EL Implantable Drug Pumps and Refill Kits General Hospital and Personal Use Devices Medtronic Inc. Switzerland SATP
Application Card software SynchroMed® II Implantable Drug Pump General Hospital and Personal Use Devices Medtronic Inc. Switzerland SATP
ISOMED Implantable Infusion Pumps (Mod. 8472-20, 8472-35, 8472-60) and SYNCHROMED II (Mod. 8637-20 and 8637-40). Anvisa registration number: 10099430095 (ISOMED) and 10099430103 (SYNCHROMED II). General Hospital and Personal Use Devices Medtronic Inc; Dabasons Imp. Exp. e Comércio Ltda Brazil ANVISA
MEDTRONIC IMPLANTABLE INFUSION PUMP. Models: SYNCHROMED II 8637-20 and 8637-40; SYNCHROMED EL 8626-10, 8626L-10, 8626-18, 8626L-18; SYNCHROMED EL 8627. Anvisa Registries No. 10339190229, 10339190104 and 10339190105. General Hospital and Personal Use Devices Medtronic Comercial Ltda. Brazil ANVISA
Implanted Infusion Pump Medtronic Technical Name: Synchromed II 8637-20 / Synchromed II 8637-40 ANVISA Registration Number: 10339190229 Hazard Class: IV Affected Model: 8637-20 and 8637-40 Serial Numbers Affected: PUMP 8637 -20 SM2 20ML EMAN US JUN BATRY; PUMP 8637-20 SM2 20ML PAP MAN US JUN BAT; PUMP 8637-20 SM2 20ML PAPER MAN USMKT SL; PUMP 8637-20 SM2 20ML PAPR MAN USMKTJUNC PUMP 8637-20 SYNCH II 20ML US MKT SL; PUMP 8637-20 SYNCHMED II 20ML PF; PUMP 8637-20 SYNCHMED II PCKT FILL L105; PUMP 8637-20 SYNCHROMED II L089; PUMP 8637-20 SYNCHROMED II OUS L105; PUMP 8637-40 SYNCHMED II PCKT FILL L105; PUMP 8637-40 SYNCHROMED II L089; PUMP 8637-40 SYNCHROMED II OUS L105. General Hospital and Personal Use Devices Medtronic Inc.; MEDTRONIC COMERCIAL LTDA Brazil ANVISA