376 results
·
19ms
·
Sources: EU EUDAMED, US FDA
INFINION 0.6T MR IMAGING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033518366·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033518380·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033518397·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033518342·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033518359·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033518335·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033518373·
MODIFICATION TO AT HOME DRUG TEST, MODELS 9150, 9068, AND 9175
FDA 510(k)
FDA Unclassified
·Unknown
VELOGENE GENOMIC IDENTIFICATION ASSAY FOR MRSA WITH ONE-STEP DETECTION
FDA 510(k)
FDA Class 2
·Microbiology
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·October 18, 2019
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·March 20, 2013
TENDRIL ST
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2011
UNK HAKIM VALVE
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC./ MEDOS S.A.·Product code JXG·March 14, 2008
NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 16, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 3, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026