7 results
·
22ms
·
Sources: EU EUDAMED, US FDA
BONE MARROW BIOPSY SYSTEM
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
VITALCARE URETHRAL CATHETER RED RUBBER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Low Profile Companion Sheath
FDA 510(k)
FDA Class 2
·Cardiovascular
GYNECARE X-TRACT MORCELLATOR
FDA Adverse Event
Injury
·ETHICON, INC.·Product code HET·June 16, 2006
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·December 8, 2010
ALTRX NEUT 36IDX54OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·January 22, 2013
RNS SYSTEM
FDA Adverse Event
Injury
·NEUROPACE, INC.·Product code PFN·July 9, 2014