7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SUB-Q-SET(R) SUBCUTANEOUS INFUSION SET
FDA 510(k)
FDA Class 2
·General Hospital
BARBED SQUARE STAPLE
FDA 510(k)
FDA Class 2
·Orthopedic
VORTECH'S FILM DIGITIZER, FD-1
FDA 510(k)
FDA Class 2
·Radiology
DRILL, AO, STERILE T2 FEMUR 4,2X340 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code HTW·December 18, 2012
CONSTELLATION VISION SYSTEM
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·January 17, 2013
VOYAGER RX CORONARY DILATATION CATHETER
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code LOX·December 14, 2010
TENDRIL STS
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI·Product code DTB·January 15, 2014