36 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VITABLOCS
FDA 510(k)
FDA Class 2
·Dental
GEN4 DIGITAL
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828113458·GEN4 DIGITAL
GEN4 DIGITAL
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828137294·GEN4 DIGITAL
GEN4 DIGITAL
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828112383·GEN4 DIGITAL
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780375210·Integra® Jarit® Metzenbaum Scissors, 11-1/4", S...
PROTECTIV ACUVANCE IV CATHETER SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
ACTIVE INHIBIN-A ELISA, MODEL DSL-10-28100
FDA 510(k)
FDA Class 1
·Clinical Chemistry
ARSTASIS ACCESS SYSTEM
FDA Adverse Event
Other
·ARSTASIS INC.·Product code DYB·November 15, 2010
ARSTASIS ACCESS SYSTEM
FDA Adverse Event
Malfunction
·ARSTASIS, INC.·Product code DYB·November 19, 2010
ARSTASIS ACCESS SYSTEM
FDA Adverse Event
Other
·ARSTASIS, INC.·Product code DYB·November 22, 2010
COZMONITOR GLUCOSE MONITOR
FDA Adverse Event
Injury
·SMITHS MEDICAL MD·Product code NBW·October 21, 2005
ARSTASIS ACCESS SYSTEM
FDA Adverse Event
Injury
·ARSTASIS, INC.·Product code DYB·November 1, 2010
NEXGEN LPS-FLEX FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code NJL·April 26, 2013
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 19, 2011
HEARTSTRING II PROXIMAL SEAL SYSTEM
FDA Adverse Event
Malfunction
·GUIDANT CARDIAC SURGERY·Product code DXC·August 7, 2008
PERCUFLEX PLUS
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORPORATION·Product code FAD·November 9, 2023
ABRE VENOUS SELF-EXPANDING STENT SYSTEM
FDA Adverse Event
Injury
·COVIDIEN·Product code QAN·March 26, 2026
GALAXY G3 MINI 2MM X 4CM
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·June 16, 2021
GALAXY G3 5MM X 15CM
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·June 16, 2021
GALAXY G3 MINI 3MM X 8CM
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·June 16, 2021