758 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Clarifi Imaging System
FDA 510(k)
FDA Class 2
·Cardiovascular
Integra® Miltex®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780362401·Integra® Miltex® Vannas Capsulotomy Scissors, 3...
SignaLoc Screw
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215116712·
SYNTHES RIB FIXATION SYSTEM
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
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011
S-ROM M HEAD 36MM +0
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 21, 2013
APEX MODULAR HIP STEM
FDA Adverse Event
Injury
·OMN LIFE SCIENCE, INC.·Product code KWY·September 29, 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
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 11, 2024