23 results · 21ms · Sources: EU EUDAMED, 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