24 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FreeStyle Libre 2 Flash Glucose Monitoring System (with FreeStyle Libre 2 App)
FDA 510(k)
FDA Class 2
·Clinical Chemistry
METAPHYSARY BROACH ESOP LEFT SIZE 16,25
FDA UDI
FOURNITURES HOSPITALIERES INDUSTRIE·03661489017612·
HHM
FDA UDI
Oticon A/S·05707131351876·G300 SC, BTE PP 13 2.4G 105 C094 TAR HHM
NA
FDA UDI
Synthes GmbH·10886982142726·2.4MM CORTEX SCREW SLF-TPNG WITH T8 STARDRIVE R...
CODMAN
FDA UDI
Cerenovus, Inc.·10886704002024·CODMAN SLIM-LINE Aneurysm Clip Graft 2mm Diamet...
Medical Facets NC
FDA UDI
MEDICAL FACETS NC LLC·M933MDF2017610·2.4mm Cortex Screw, T8 Stardrive, Self-Tapping,...
PREMIER ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
STATLYTE NA/K/CL/LI ANALYZER
FDA 510(k)
FDA Class 2
·Clinical Chemistry
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 29, 2025
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·July 20, 2023
SIGTIBCEMSTM 13X30 1.5/2/2.5/3
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JWH·January 29, 2018
GE OEC 9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 21, 2008
TARGET TIP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 2, 2013
ANIMAS INSULIN CARTRIDGE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·April 9, 2012
PULSE-GENERATOR, PACEMAKER, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DXY·December 7, 2017
AXIOS STENT AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code PCU·February 15, 2017
PULSE-GENERATOR, PACEMAKER, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DXY·December 7, 2017
PULSE-GENERATOR, PACEMAKER, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DXY·December 7, 2017
HEARTWARE VENTRICULAR ASSIST SYSTEM-PUMP
FDA Adverse Event
Death
·HEARTWARE, INC.·Product code DSQ·December 7, 2017