23 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IT-7 FEMORAL COMPONENT, ANATOMIC HIP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
POWER-V PICC 5 FR SINGLE LUMEN
FDA Adverse Event
Injury
·NEOMEDICAL, INC·Product code LJS·October 15, 2010
POWER-V PICC 5 FR SINGLE LUMEN
FDA Adverse Event
Injury
·NEOMEDICAL, INC.·Product code LJS·October 15, 2010
POWER-V PICC 5 FR SINGLE LUMEN
FDA Adverse Event
Injury
·NEOMEDICAL, INC·Product code LJS·October 15, 2010
POWER-V PICC 5 FR SINGLE LUMEN
FDA Adverse Event
Injury
·NEOMEDICAL, INC·Product code LJS·October 15, 2010
POWER-V PICC 5 FR SINGLE LUMEN
FDA Adverse Event
Injury
·NEOMEDICAL, INC·Product code LJS·October 15, 2010
POWER-V PICC 5 FR SINGLE LUMEN
FDA Adverse Event
Injury
·NEOMEDICAL, INC.·Product code LJS·October 15, 2010
POWER-V PICC 5 FR SINGLE LUMEN
FDA Adverse Event
Injury
·NEOMEDICAL, INC·Product code LJS·October 15, 2010
V-CATH
FDA Adverse Event
Other
·HDC CORP.·Product code LJS·August 29, 2006
REMOTE CONTROLLED X-RAY DIAGNOSTIC RS-110
FDA 510(k)
FDA Class 2
·Radiology
ESCORT-LINK ARRHYTHMIA OPTION 23L
FDA 510(k)
FDA Class 2
·Cardiovascular
V-CATH
FDA Adverse Event
Other
·HDC CORP.·Product code DQO·August 28, 2006
2925153-2000-00007
FDA Adverse Event
Other
·Product code DQO·June 24, 2000
2925153-2000-00004
FDA Adverse Event
Other
·Product code DQO·June 24, 2000
2925153-2000-00002
FDA Adverse Event
Injury
·Product code DQO·March 14, 2000
2925153-2000-00018
FDA Adverse Event
Injury
·Product code ---·January 29, 2001
2925153-2000-00017
FDA Adverse Event
Injury
·Product code ---·March 12, 2001
2925153-2001-00009
FDA Adverse Event
Injury
·Product code HOC·June 30, 2001
V-CATH
FDA Adverse Event
Injury
·HDC CORP.·Product code DQO·September 29, 1998
SOLETRA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·January 22, 2013