20 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FDA 510(k)
FDA Class 2
·Cardiovascular
Eagle Derma2 Nitrile Examination Gloves
FDA UDI
Eagle Protect Pbc·09421024254155·Derma2 Nitrile Examination Gloves, Blue, Powder...
ProLift
FDA UDI
Life Spine, Inc.·00190837117580·
ZB ProLift Narrow
FDA UDI
Life Spine, Inc.·00190837079321·
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321515120·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311515120·
CAC-127-8 CARDOAC ARRAY COIL
FDA 510(k)
FDA Class 2
·Radiology
MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, WATCHBP OFFICE TARGET (BP3MD1-4).
FDA 510(k)
FDA Class 2
·Cardiovascular
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·January 11, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·January 11, 2019
PENUMBRA SMART COIL
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code HCG·December 11, 2015
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·March 13, 2019
UPBITING PITUITARY
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·October 8, 2014
WALLFLEX? ESOPHAGEAL
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code ESW·June 7, 2013
BIPOLAR WORKING ELEMENT
FDA Adverse Event
Malfunction
·RICHARD WOLF MEDICAL INSTRUMENTS·Product code GEI·June 23, 2011
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·April 10, 2019
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code OLO·February 22, 2019
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code OLO·March 11, 2019
UNK GEL BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FTR·May 27, 2020
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·April 3, 2019