7 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
DISPOSABLE MICROSTAAR INJECTOR
FDA 510(k)
FDA Class 1
·Ophthalmic
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471150690·K-WIRE - SINGLE TROCAR 0.9mm DIA x 75mm
PERIARTICULAR LOCKING PLATES AND SCREWS, 2358, 2359 SERIES
FDA 510(k)
FDA Class 2
·Orthopedic
ADVANCE SALIVARY BALLOON CATHETER WITH WIRE GUIDE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
INRATIO PT/INR TEST STRIPS
FDA Adverse Event
Injury
·ALERE SAN DIEGO, INC.·Product code GJS·June 18, 2014
LAMITRODE 88
FDA Adverse Event
Injury
·ST. JUDE MEDICAL- NEUROMODULATION·Product code LGW·January 29, 2013
EON MINI RECHARGEABLE IPG
FDA Adverse Event
Injury
·ST JUDE MEDICAL- NEUROMODULATION DIVISION·Product code LGW·December 21, 2010