28 results
·
28ms
·
Sources: EU EUDAMED, US FDA
MORTARA ELI 10 ELECTROCARDIOGRAPH
FDA 510(k)
FDA Class 2
·Cardiovascular
K090539
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·February 26, 2026
NYLON NONABSORBABLE SURGICAL SUTURES, USP
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TIPOWER POWERDRIVE AND RIMPOWER X & SX
FDA 510(k)
FDA Class 2
·Physical Medicine
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·June 12, 2018
VYPRO MESH UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·June 12, 2018
BIPAP AUTOSV ADV
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 20, 2022
BIPAP AUTOSV ADVANCED
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 20, 2022
BIPAP AUTOSV ADV
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 20, 2022
DREAMSTATION BIPAP AUTOSV
FDA Adverse Event
Injury
·RESPIRONICS, INC.·Product code MNS·January 16, 2023
BIPAP AUTOSV ADV
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 20, 2022
BIPAP AUTOSV ADV SYSTEM ONE
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 21, 2022
BIPAP AUTOSV ADV
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 12, 2026
BIPAP AUTOSV ADV
FDA Adverse Event
Malfunction
·RESPIRONICS INC·Product code MNS·October 31, 2022
6.0MM TI MATRIX SCREW 45MM THREAD LENGTH
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code NKB·April 22, 2013
ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·March 29, 2011
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·July 1, 2008
BIPAP AUTOSV ADVANCED SYSTEM
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·January 28, 2022
DREAMSTATION BIPAP AUTOSV
FDA Adverse Event
Malfunction
·RESPIRONICS INC·Product code MNS·November 1, 2022
BIPAP AUTOSV ADV
FDA Adverse Event
Malfunction
·RESPIRONICS INC·Product code MNS·November 7, 2022