747 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Penumbra System 110 Aspiration Tubing
FDA 510(k)
FDA Class 2
·Cardiovascular
PENUMBRA SYSTEM MAX ASPIRATION TUBING
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code NRY·June 24, 2015
Masel
FDA UDI
Ortho Organizers, Inc.·00190707040932·Choice™ Torquing Pliers - Male
ProLift
FDA UDI
Life Spine, Inc.·00190837105884·Static Expandable Cage Trial, 12mm x 28mm x 7mm...
ANATOMICAL SHOULDER KEELED GLENOID
FDA 510(k)
FDA Class 2
·Orthopedic
INQUIRY AFOCUSII DIAGNOSTIC CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 12, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 11, 2024
BIPAP A40
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 9, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 6, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 13, 2024
TBD
FDA Adverse Event
Injury
·MPRI·Product code LWP·June 7, 2013
UNICEL DXC 800 SYNCHRON SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·June 24, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·September 10, 2008
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 16, 2024
BIPAP A40 PRO, IT
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 5, 2025
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·June 5, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·June 6, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·June 5, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 11, 2024