8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
DOPSCAN MODEL 1050
FDA 510(k)
FDA Class 2
·Cardiovascular
Snowden-Pencer
FDA UDI
STERIS CORPORATION·10885403151439·Snowden-Pencer RETRACTOR DESMARRES LID, INSULAT...
VERDICT -II BAR/BZO
FDA 510(k)
FDA Class 2
·Clinical Toxicology
FORTROSS BONE VOID FILLER
FDA 510(k)
FDA Class 2
·Orthopedic
GMK-REVISION FEMUR REVISION PS #4 R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·August 23, 2021
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 16, 2014
SPRINT
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 31, 2012
TECNIS 1-PIECE
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HQL·August 22, 2010