18 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BROWNE CIDEX OPA INDICATOR
FDA 510(k)
FDA Class 2
·General Hospital
MULTI-MED CENTRAL VENOUS CATHETERS, MODELS: M3720HKIC, M4820HKIC
FDA 510(k)
FDA Class 2
·General Hospital
V-STRUT Vertebral Implant
FDA 510(k)
FDA Class 2
·Orthopedic
MICROTAINER SST GOLD
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·June 7, 2018
BD MICROTAINER® EDTA LAVENDAR TUBES
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·May 1, 2018
BD MICROTAINER® EDTA LAVENDAR TUBES
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·May 16, 2018
MICROTAINER SST GOLD
FDA Adverse Event
Malfunction
·BECTON DICKINSON CARIBE LTD·Product code JKA·May 7, 2018
BD MICROTAINER® EDTA LAVENDER TUBES
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·April 27, 2018
BD MICROTAINER® EDTA LAVENDAR TUBES
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·May 3, 2018
BD MICROTAINER® BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·December 3, 2017
CONSERVE(R) TOTAL HEAD W/BFH
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·March 6, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MPRI·Product code DTB·August 8, 2014
SPRINT QUATTRO SECURE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·October 15, 2025
TRUESPAN 24 DEGREE PEEK
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SÃ RL·Product code MBI·October 29, 2018
TRUESPAN 12 DEGREE PEEK
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SÃ RL·Product code MBI·October 29, 2018
TRUESPAN 12 DEGREE PEEK
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SÃ RL·Product code MBI·October 29, 2018
TRUESPAN 12 DEGREE PEEK
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SÃ RL·Product code MBI·October 29, 2018