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COR25000318-000

FDA Adverse Event
No answer provided ·Product code REQ·August 1, 2025

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code LXH·August 7, 2023

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code LXH·September 11, 2020

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code LXH·July 24, 2020

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code LXH·September 14, 2020

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code LXH·September 11, 2020

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code LXH·September 14, 2020

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code FZT·September 11, 2020

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code LXH·September 11, 2020

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code LXH·September 14, 2020

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code LXH·September 14, 2020

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code FZT·September 11, 2020

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code LXH·December 29, 2020

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code LXH·December 29, 2020

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code LXH·September 14, 2020

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code LXH·June 25, 2024

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code LXH·August 3, 2022

GRAFT PREP SYS SLIDERUNIT (2 REQ) *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code LXH·August 3, 2022

CARPENTIER - EDWARDS BIOPROSTHESIS

FDA Adverse Event
Other ·EDWARDS LIFESCIENCES·Product code DYE·June 13, 2008

ABBOTT

FDA Adverse Event
Injury ·ABBOTT LABS, HOSPITAL PRODUCTS DIVISION·Product code FRN·October 12, 2001