9 results
·
32ms
·
Sources: EU EUDAMED, US FDA
PLASTIC TUBING CONNECTORS
FDA 510(k)
FDA Class 2
·General Hospital
CROSSPOINT TRANSACCESS CATHETER, MODEL TA-XP-001
FDA 510(k)
FDA Class 2
·Radiology
STABILIZATION SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
LAMITRODE S8
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·March 6, 2014
3.0MM TI STERNAL LCKNG SCREW SELF-DRILLING/14MM
FDA Adverse Event
Injury
·Product code HWC·November 14, 2012
REPLY
FDA Adverse Event
Malfunction
·SORIN BIOMEDICA CRM S.R.L.·Product code NVZ·September 7, 2010
PULSESELECT
FDA Adverse Event
Malfunction
·MEDTRONIC CRYOCATH LP·Product code QZI·October 1, 2025
PV-TRACKER GUIDE WIRE
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code DQX·November 26, 2025
PV-TRACKER GUIDE WIRE
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code DQX·September 26, 2025