10 results
·
17ms
·
Sources: EU EUDAMED, US FDA
TELEMETRY RECEIVER ACCESSORY FOR THE CMS 8000
FDA 510(k)
FDA Class 2
·Cardiovascular
CD HORIZON® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994291394·SCREW 7894540 CDH PEEK 4.5X40 NON CANN
Precept
FDA UDI
Nuvasive, Inc.·00887517385987·PRECEPT Screw Shank, 4.5x40mm Modular
MEGA PLUS MIS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809916497001·Long-arm Multi-Axial Fenestrated Screw, Ø4.5 x ...
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·June 23, 2024
CYSTINE TRYPTIC AGAR W/FRUCTOSE
FDA 510(k)
FDA Class 1
·Microbiology
OP-CON SURGICAL INSTRUMENT #9
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
CAPTURE-R READY-SCREEN (3)
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·June 25, 2014
ALLEGRETTO WAVE EYE-Q EXCIMER LASER
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·July 7, 2015
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code CBK·December 27, 2012