10 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TITAN GEL IMMUNOFIX-9 CAT. NO. 3051 AND 3067
FDA 510(k)
FDA Class 2
·Immunology
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471144330·PASSING PIN - DRILL TIP 2.4mm DIA x 385mm
MULTIBOLUS II DISPOSABLE PAIN MANAGEMENT SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
CARDIOBLATE BIPOLAR RADIOFREQUENCY SURGICAL ABLATION SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SURGICEL* 5X7.5CM
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code LMG·December 23, 2020
MOSAIC MITRAL BIOPROSTHETIC VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code DYE·December 17, 2019
HANCOCK II MITRAL BIOPROSTHETIC HEART VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code DYE·December 17, 2019
SPACELABS ULTRAVIEW PATIENT MONITOR
FDA Adverse Event
Death
·SPACELABS HEALTHCARE INC.·Product code MHX·June 20, 2014
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·January 28, 2013
PFC SIGMARP CV TB/IN S4 10.0
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code NJL·December 15, 2010