9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SMARTBOND
FDA 510(k)
FDA Class 2
·Dental
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074088525·INSTRUMENT 2981036 10X36MM DSTRCTR TRIAL
Polystar Selection EDITION
FDA UDI
Merz Dental GmbH·D7091981036·anteriors; shade A2; mould BS2
AUTO-SYRINGE INFUSION SET
FDA 510(k)
FDA Class 2
·General Hospital
4D INTEGRATED TREATMENT CONSOLE WITH PATIENT ACCESSORY VERIFICATION SYSTEM (PAVS)
FDA 510(k)
FDA Class 2
·Radiology
ETEST FOSFOMYCIN FM 1024 WW B30
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code JWY·April 16, 2020
STRAIGHT SUCTION, AXIEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·February 27, 2013
MECHANICAL WALKER, ROLLATOR
FDA Adverse Event
CONSMA·Product code ITJ·August 5, 2014
SENSOR ENLITE
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OZO·September 27, 2016