Medos International Sàrl
1,963 devices · 39,868 adverse event reports · 61 deaths reported · 10 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- ORBIT GALAXY ENPOWER 641CF0306DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- ORBIT GALAXY ENPOWER 641CF0615DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- RAPIDTRANSIT 601-231Catheter, continuous flush1 report
- RAPIDTRANSIT 601-240Catheter, continuous flush1 report
- RAPIDTRANSIT 601-251Catheter, continuous flush1 report
- PROWLER 606-051FXCatheter, continuous flush1 report
- PROWLER 606-051XCatheter, continuous flush1 report
- PROWLER 606-151JXCatheter, continuous flush1 report
- PROWLER 606-2510Catheter, continuous flush1 report
- PROWLER 606-2510XCatheter, continuous flush1 report
- PROWLER SELECT 606-S252XCatheter, continuous flush1 report
- ORBIT GALAXY 640CF0201DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- ORBIT GALAXY 640CF0505DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- ORBIT GALAXY 640CF0610DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- ORBIT GALAXY 640CF0715DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- ORBIT GALAXY 640CF0815DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- ORBIT GALAXY 640CF1230DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- ORBIT GALAXY 640CR1030DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- ORBIT GALAXY 640CR1430DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- ORBIT GALAXY 640CR1630Device, Vascular, for Promoting Embolization1 report
- ORBIT GALAXY 640CR2030Device, Vascular, for Promoting Embolization1 report
- ORBIT GALAXY XTRASOFT 640CX0404Device, Vascular, for Promoting Embolization1 report
- NA 91-4205USPUMP, INFUSION, IMPLANTED, PROGRAMMABLE1 report
- ENVOY 671-256-05DBCATHETER, PERCUTANEOUS1 report
- NA 82-6881DEVICE, MONITORING, INTRACRANIAL PRESSURE1 report
- CODMAN CERTAS 82-8802PLShunt, central nervous system and components1 report
- CODMAN CERTAS SIPHONGUARD 82-8805PLShunt, central nervous system and components1 report
- CODMAN CERTAS SIPHONGUARD 82-8806PLShunt, central nervous system and components1 report
- YOGA MC24150ZBCATHETER, PERCUTANEOUS1 report
- CODMAN VersaTru 9008050SLELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- CODMAN CERTAS SIPHONGUARD 82-8815PLShunt, central nervous system and components1 report
- CODMAN CERTAS SIPHONGUARD 82-8826PLShunt, central nervous system and components1 report
- GRYPHON 211038ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- RIGIDFIX 213704APPLIER, STAPLE, SURGICAL,1 report
- RIGIDFIX 213717Guide, surgical, instrument1 report
- NA 213816Guide, surgical, instrument1 report
- NA 213818Guide, surgical, instrument1 report
- NA 214105ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- NA 214123CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- GII 214542REAMER1 report
- NA 214562Guide, surgical, instrument1 report
- NA 214606ACCESSORIES,ARTHROSCOPIC1 report
- NA 214608ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- NA 214612ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- NA 214617ACCESSORIES,ARTHROSCOPIC1 report
- NA 214621ACCESSORIES,ARTHROSCOPIC1 report
- NA 214681ACCESSORIES,ARTHROSCOPIC1 report
- NA 214711ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- NA 215402TRAY, SURGICAL, INSTRUMENT1 report
- NA 215451TRAY, SURGICAL, INSTRUMENT1 report
- NA 219204ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- RESTORE 219343REAMER1 report
- RESTORE 219351ACCESSORIES,ARTHROSCOPIC1 report
- NA 219443ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- NA 219444ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- NA 219447ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- RESTORE 219551REAMER1 report
- NA 219959ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- NA 219963ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- NA 219965ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- HEALIX PEEK ORTHOCORD 222219Screw, fixation, bone1 report
- ORTHOCORD HEALIX TI 222241Screw, fixation, bone1 report
- ORTHOCORD HEALIX TI 222248STAPLE, FIXATION, BONE1 report
- HEALIX TRANSTEND ORTHOCORD PERCANNULA 222261Screw, fixation, bone1 report
- ORTHOCORD 223105SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE1 report
- ORTHOCORD 228144SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE1 report
- RAPIDLOC 228301ACCESSORIES,ARTHROSCOPIC1 report
- PROFILE 230320Screw, fixation, bone1 report
- PROFILE 230520Screw, fixation, bone1 report
- PROFILE 230525Screw, fixation, bone1 report
- RESTORE 232015ACCESSORIES,ARTHROSCOPIC1 report
- NA 232407REAMER1 report
- NA 232415REAMER1 report
- NA 232417REAMER1 report
- NA 232418REAMER1 report
- NA 232420REAMER1 report
- NA 232421REAMER1 report
- CLEARFIX 253110ACCESSORIES,ARTHROSCOPIC1 report
- CLEARFIX 253111ACCESSORIES,ARTHROSCOPIC1 report
- CLEARFIX 253113ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- NA 254605ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- RIGIDFIX 213027FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE1 report
- PERCANNULA 222274CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- HEALIX ADVANCE ORTHOCORD 222302FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE1 report
- HEALIX ADVANCE ORTHOCORD 222321Screw, fixation, bone1 report
- HEALIX ADVANCE ORTHOCORD 222322Screw, fixation, bone1 report
- HEALIX ADVANCE ORTHOCORD 222324FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE1 report
- NA 260011ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- NA 219974ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- MILAGRO 231828FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE1 report
- HEALIX ADVANCE 222328ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- HEALIX ADVANCE 222329ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- RIGIDLOOP 232018FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE1 report
- RIGIDLOOP 232021FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE1 report
- RIGIDLOOP 232030ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- ORTHOCORD 223125SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE1 report
- ORTHOCORD 223127SUTURE, SURGICAL, ABSORBABLE, POLYDIOXANONE1 report
- ORTHOCORD 223121SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE1 report
- MILAGRO 231832Screw, fixation, bone1 report
- NA 214015ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report