117 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SYNCHRON SYSTEMS SALICYLATE REAGENT AND CALIBRATOR
FDA 510(k)
FDA Class 2
·Clinical Toxicology
CARDINAL HEALTH
FDA UDI
Cardinal Health 200, LLC·10885425813445·IV START KIT
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033568910·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033568897·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033568934·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033568903·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033568941·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033568880·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033568927·
Clever Choice Comfort EZ
FDA UDI
SIMPLE DIAGNOSTICS INC·00898302141732·Insulin Pen Needle 32G and 3/16 inch (5 mm) length
SNAZZY2
FDA 510(k)
FDA Class 2
·Physical Medicine
TELEPAX
FDA 510(k)
FDA Class 2
·Radiology
OT VERIO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 21, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·March 10, 2011
ICY HOT HEAT THERAPY PATCH
FDA Adverse Event
Other
·CHATTEM, INC.·Product code IMD·March 13, 2008
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·January 16, 2025
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026