11 results
·
25ms
·
Sources: EU EUDAMED, US FDA
FDR D-EVO FLAT PANEL DETECTOR SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304010147·
Bernafon
FDA UDI
Bernafon AG·05711584053041·JU9 ITCPD, WL R BE JUNA 9
KYPHON ANCHOR FACET SCREW SYSTEM
FDA 510(k)
FDA Unclassified
·Unknown
FULL CORE BIOPSY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PLEURX LOCKABLE DRAINAGE LINE SET
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code DWM·April 2, 2026
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·October 4, 2014
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·June 27, 2011
PLEURX
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code DWM·September 26, 2025
PLEURX
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code DWM·June 2, 2025