24 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
RT-PLUS MODULAR CEMENTED KNEE COMPONENTS
FDA 510(k)
FDA Class 2
·Orthopedic
Creation Willi Geller
FDA UDI
KLEMA Dentalprodukte GmbH·ECWG0035041·CC/ Transition Dentine TD-A3,5
Creation Willi Geller
FDA UDI
KLEMA Dentalprodukte GmbH·09010782023792·CC/ Transition Dentine TD-A3,5
ADVANTA SUPER SOFT GRAFT
FDA 510(k)
FDA Class 2
·Cardiovascular
OSCAR 2, MODEL 222
FDA 510(k)
FDA Class 2
·Cardiovascular
Spacelabs Healthcare
FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522124891·4 ELECTRODE EVO, BELT MOUNTED, PACKED ITALIAN
NA
FDA UDI
STRYKER CORPORATION·04546540046635·Thin Offset (17.5 x 0.38 x 34.5mm)
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 13, 2024
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL UM-D·Product code FPA·February 20, 2025
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL UM-D·Product code FPA·February 20, 2025
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·January 6, 2025
ALLURA XPER FD
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·April 18, 2025
2520274-2013-11008
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code KWQ·February 28, 2013
STERLING BALLOON DILATATION CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·March 1, 2011
INDURA CATHETER
FDA Adverse Event
Malfunction
·RICE CREEK MANUFACTURING·Product code LKK·February 21, 2008
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 9, 2024
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 9, 2024
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 9, 2024
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 9, 2024
PINNACLE SECTOR II CUP 60MM
FDA Adverse Event
Injury
·. DEPUY ORTHOPAEDIC INC, 1818910·Product code KWA·May 25, 2018