10 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
THERAPEP
FDA 510(k)
FDA Class 2
·Anesthesiology
REBOUND HRD
FDA Adverse Event
Malfunction
·MINNESOTA MEDICAL DEVELOPMENT, INC.·Product code FTL·May 16, 2011
REBOUND HRDV
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Roadrunner Extra Support Wire Guide
FDA 510(k)
FDA Class 2
·Cardiovascular
HEARTSTART XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 27, 2014
PROLIFT PELVIC FLOOR REPAIR
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTP·February 28, 2013
APEX MONORAIL 3.5X12
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code LOX·February 1, 2011
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·July 26, 2024
ROADRUNNER EXTRA-SUPPORT BARE MANDRIL WIRE GUIDE
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·November 23, 2021
ROADRUNNER EXTRA-SUPPORT BARE MANDRIL WIRE GUIDE
FDA Adverse Event
Injury
·COOK INC·Product code DQX·January 30, 2023